97- Machine Learning in Computational NMR-aided Structural Elucidation
Cortés, I.; Cuadrado, C.; Herández Daranas, A.*; Sarotti, A. M.*
Frontiers in Natural Products, 2, 2023 (2023)
doi: doi.org/10.3389/fntpr.2023.1122426
Cortés, I.; Cuadrado, C.; Herández Daranas, A.*; Sarotti, A. M.*
Frontiers in Natural Products, 2, 2023 (2023)
doi: doi.org/10.3389/fntpr.2023.1122426
96- Chemical stability of petrichorins
Li, C.; Sarotti, A. M.; Herández Daranas, A.; Wu, X.; Zheng, S-L.; Blodgett, J.; Cao, S.*
J. Org. Chem., 87, 16847-16850 (2022)
doi: 10.1021/acs.joc.2c01275
Li, C.; Sarotti, A. M.; Herández Daranas, A.; Wu, X.; Zheng, S-L.; Blodgett, J.; Cao, S.*
J. Org. Chem., 87, 16847-16850 (2022)
doi: 10.1021/acs.joc.2c01275
95- May the force (field) be with you: on the importance of conformational searches in the prediction of NMR chemical shifts
Cuadrado, C.; Herández Daranas, A.*, Sarotti, A. M.*
Marine Drugs, 20, 699 (2022)
doi: 10.3390/md20110699
Cuadrado, C.; Herández Daranas, A.*, Sarotti, A. M.*
Marine Drugs, 20, 699 (2022)
doi: 10.3390/md20110699
94- Towards the Synthesis of Highly Hindered Pyrrolidines by Intramolecular AAC Click Reactions: What Can Be Learned from DFT Calculations?
Cicetti, S.; Maestre, E.; Spanevello, R. A.; Sarotti, A. M.*
Eur. J. Org. Chem., e200200478 (2022)
doi: 10.1002/ejoc.202200478
Cicetti, S.; Maestre, E.; Spanevello, R. A.; Sarotti, A. M.*
Eur. J. Org. Chem., e200200478 (2022)
doi: 10.1002/ejoc.202200478
93- "ML-J-DP4: an integrated quantum mechanics-machine learning approach for ultra-fast NMR structural elucidation”
Tsai, Y. H.; Amichetti, M.; Zanardi, M. M.; Grimson, R.; Herández Daranas, A.; Sarotti, A. M.*
Org. Lett., 24, 7487-7491 (2022)
doi: 10.1021/acs.orglett.2c01251
Tsai, Y. H.; Amichetti, M.; Zanardi, M. M.; Grimson, R.; Herández Daranas, A.; Sarotti, A. M.*
Org. Lett., 24, 7487-7491 (2022)
doi: 10.1021/acs.orglett.2c01251
92- "Discovery of unusual dimeric piperazyl cyclopeptides encoded by a Lentzea flaviverrucosa DSM 44664 biosynthetic supercluster”
Li, C.; Hu, Y.; Wu, X.; Stumpf, S. D.; Qi, S.; D´Alessandro, J. M.; Nepali, K. K.; Sarotti, A. M.; Cao, S.*; Blodgett, J. A. V.
Proc. Natl. Acad. Sci. (PNAS), 119, e2117941119 (2022)
doi: 10.1073/pnas.2117941119
Li, C.; Hu, Y.; Wu, X.; Stumpf, S. D.; Qi, S.; D´Alessandro, J. M.; Nepali, K. K.; Sarotti, A. M.; Cao, S.*; Blodgett, J. A. V.
Proc. Natl. Acad. Sci. (PNAS), 119, e2117941119 (2022)
doi: 10.1073/pnas.2117941119
91- "New and bioactive polyketides from Hawaiian marine-derived fungus Trichoderma sp. FM652”
Uz Zaman, K. H. A.; Wu, X.; Sarotti, A. M.,; Cao, S.*
Nat. Prod. Res., 36, 5984-5990 (2022)
doi: 10.1080/14786419.2022.2056890
Uz Zaman, K. H. A.; Wu, X.; Sarotti, A. M.,; Cao, S.*
Nat. Prod. Res., 36, 5984-5990 (2022)
doi: 10.1080/14786419.2022.2056890
90- "Polyketides, diketopiperazines and an isochromanone from the marinederived fungal strain Fusarium graminearum FM1010 from Hawaii"
Uz Zaman, K. H. A., Sarotti, A. M., Wu, W.; Cao, S.*
Phytochemistry, 198, 113183 (2022)
doi: 10.1016/j.phytochem.2022.113138
Uz Zaman, K. H. A., Sarotti, A. M., Wu, W.; Cao, S.*
Phytochemistry, 198, 113183 (2022)
doi: 10.1016/j.phytochem.2022.113138
89- "BOPHY-fullerene C60 dyad as a photosensitizer for antimicrobial photodynamic therapy"
Gonzalez, E. J., Sarotti, A. M., Martínez, S. R.; Macor, L. P.; Durantini, J. E.; Renfige, M.; Gervaldo, M. A.; Otero, L. A.; Durantini, A. M.; Durantini, E. N.; Heredia, E. A.*
Chem. Eur. J., 8, e2002103884 (2022)
doi: 10.1002/chem.202103884
Gonzalez, E. J., Sarotti, A. M., Martínez, S. R.; Macor, L. P.; Durantini, J. E.; Renfige, M.; Gervaldo, M. A.; Otero, L. A.; Durantini, A. M.; Durantini, E. N.; Heredia, E. A.*
Chem. Eur. J., 8, e2002103884 (2022)
doi: 10.1002/chem.202103884
88- "A Critical Review on the Use of DP4+ in the Structural Elucidation of Natural Products: The Good, The Bad and The Ugly. A Practical Guide"
Marcarino, M. O.; Cicetti, S.; Zanardi, M. M.;* Sarotti, A. M.*
Nat. Prod. Rep., 39, 58-76 (2022)
doi: 10.1039/D1NP00030F
Marcarino, M. O.; Cicetti, S.; Zanardi, M. M.;* Sarotti, A. M.*
Nat. Prod. Rep., 39, 58-76 (2022)
doi: 10.1039/D1NP00030F
87- "Thermal decomposition of hexamethylenetetramine: mechanistic study and identification of reaction intermediates via a computational and NMR approach"
Simonetti, S. O.*, Kaufman, T. K.; Rasia, R. M.; Sarotti, A. M.; Grimblat, N.*
Org. Biomol. Chem., 19, 7374-7378 (2021)
doi: 10.1039/D1OB01522B
Simonetti, S. O.*, Kaufman, T. K.; Rasia, R. M.; Sarotti, A. M.; Grimblat, N.*
Org. Biomol. Chem., 19, 7374-7378 (2021)
doi: 10.1039/D1OB01522B
86- "New alkaloids from a Hawaiian fungal strain Aspergillus felis FM324"
Wang, C.; Sarotti, A. M.; Uz Zaman, K. H. A.; Wu, X.; Cao, S.*
Frontiers in Chemistry, 9, 724617 (2021)
doi: 10.3389/fchem.2021.724617
Wang, C.; Sarotti, A. M.; Uz Zaman, K. H. A.; Wu, X.; Cao, S.*
Frontiers in Chemistry, 9, 724617 (2021)
doi: 10.3389/fchem.2021.724617
85- "NF-κB inhibitory, antimicrobial and antiproliferative potentials of compounds from Hawaiian fungus Aspergillus polyporicola FS910"
Wang, C.; Uz Zaman, K. H. A.; Sarotti, A. M.; Wu, X.; Zheng, S-L.; Cao, S.*
3BIOTECH, 11, 1-9 (2021)
doi: 10.1007/s13205-021-02877-7
Wang, C.; Uz Zaman, K. H. A.; Sarotti, A. M.; Wu, X.; Zheng, S-L.; Cao, S.*
3BIOTECH, 11, 1-9 (2021)
doi: 10.1007/s13205-021-02877-7
84- "On the sensitivity analysis of DP4+ with the probability distribution terms. Development of a universal and customizable method"
Zanardi, M. M.; Sarotti, A. M.*
J. Org. Chem. 86, 8544-8548 (2021)
doi: 10.1021/acs.joc.1c00987
Zanardi, M. M.; Sarotti, A. M.*
J. Org. Chem. 86, 8544-8548 (2021)
doi: 10.1021/acs.joc.1c00987
83- "BF3.OEt2-Catalyzed Unexpected Stereoselective Formation of 2,4-trans-Diallyl-2-methyl-6-aryltetrahydro-2H-pyrans with Quaternary Stereocenters"
Reddy, D. S.; Srinivas, B.; Rachineni, K.; Jagadeesh, B.; Sarotti, A. M.; Mohapatra, D. K.*
J. Org. Chem. 86, 6518-6527 (2021)
doi: 10.1021/acs.joc.1c00352
Reddy, D. S.; Srinivas, B.; Rachineni, K.; Jagadeesh, B.; Sarotti, A. M.; Mohapatra, D. K.*
J. Org. Chem. 86, 6518-6527 (2021)
doi: 10.1021/acs.joc.1c00352
82- "Are computational methods useful for structure elucidation of large and flexible molecules? Belizentrin as a case study"
Hernández Daranas, A.;* Sarotti, A. M.*
Org. Lett. 23, 503-507 (2021)
doi: 10.1021/acs.orglett.0c04016
Hernández Daranas, A.;* Sarotti, A. M.*
Org. Lett. 23, 503-507 (2021)
doi: 10.1021/acs.orglett.0c04016
81- "In silico reassignment of (+)-diplopyrone by NMR calculations. Use of a DP4/J-DP4/DP4+/DIP tandem to revise both relative and absolute configuration"
Sarotti, A. M.*
J. Org. Chem. 85, 11566-11570 (2020)
doi: 10.1021/acs.joc.0c01563
Sarotti, A. M.*
J. Org. Chem. 85, 11566-11570 (2020)
doi: 10.1021/acs.joc.0c01563
80- "NMR calculations with quantum methods: development of new tools for structural elucidation and beyond"
Marcarino, M. O.; Zanardi, M. M.; Cicetti, S.; Sarotti, A. M.*
Acc. Chem. Res. 53, 1922-1932 (2020)
doi: 10.1021/acs.accounts.0c00365
Marcarino, M. O.; Zanardi, M. M.; Cicetti, S.; Sarotti, A. M.*
Acc. Chem. Res. 53, 1922-1932 (2020)
doi: 10.1021/acs.accounts.0c00365
79- "Re-engineering organocatalysts for asymmetric Friedel-Crafts alkylation of indoles through computational studies"
Gerosa, G. G.; Marcarino, M. O.; Spanevello, R. A.; Suárez, A. G.; Sarotti, A. M.*
J. Org. Chem. 85, 9969-9978 (2020)
doi: 10.1021/acs.joc.0c01256
Gerosa, G. G.; Marcarino, M. O.; Spanevello, R. A.; Suárez, A. G.; Sarotti, A. M.*
J. Org. Chem. 85, 9969-9978 (2020)
doi: 10.1021/acs.joc.0c01256
78- "Waikikiamides A-C: Complex Diketopiperazine Dimer and Diketopiperazine-polyketide Hybrids from a Hawaiian Marine Fungal Strain Aspergillus sp. FM242"
Wang, F.; Sarotti, A. M.; Jiang, G.; Huguet-Tapia, J. C.; Zheng, S.-L.; Wu, X.; Li, C.; Ding, Y.*; Cao, S.
Org. Lett. 22, 3561-3565 (2020)
doi: 10.1021/acs.orglett.0c01411
Wang, F.; Sarotti, A. M.; Jiang, G.; Huguet-Tapia, J. C.; Zheng, S.-L.; Wu, X.; Li, C.; Ding, Y.*; Cao, S.
Org. Lett. 22, 3561-3565 (2020)
doi: 10.1021/acs.orglett.0c01411
77- "Design, synthesis and evaluation of novel levoglucosenone derivatives as promising anticancer agents"
Tsai, Y.H.; Borini Etichetti, C. M.; Cicetti, S.; Girardini, J. E. Spanevello, R. A. ; Suárez, A. G; Sarotti, A. M.*
Bioorg. Med. Chem. Lett. 30, 127247 (2020)
doi: 10.1016/j.bmcl.2020.127247
Tsai, Y.H.; Borini Etichetti, C. M.; Cicetti, S.; Girardini, J. E. Spanevello, R. A. ; Suárez, A. G; Sarotti, A. M.*
Bioorg. Med. Chem. Lett. 30, 127247 (2020)
doi: 10.1016/j.bmcl.2020.127247
76- "The risks of automation. A study of DFT energy miscalculations and its consequences in NMR-based structural elucidation"
Marcarino, M. O.; Zanardi, M. M.; Sarotti, A. M.*
Org. Lett. 22, 3561-3565 (2020)
doi: 10.1021/acs.orglett.0c01001
Marcarino, M. O.; Zanardi, M. M.; Sarotti, A. M.*
Org. Lett. 22, 3561-3565 (2020)
doi: 10.1021/acs.orglett.0c01001
75- "Quantum chemical computation and machine learning in NMR (Editorial Special Issue)"
Sarotti, A. M.*
Magn. Reson. Chem. in press (2020)
doi: 10.1002/mrc.5016
Sarotti, A. M.*
Magn. Reson. Chem. in press (2020)
doi: 10.1002/mrc.5016
74- "Looking at the big picture in Activation Strain Model/Energy Decomposition Analysis: the case of the ortho-para regioselectivity rule in Diels-Alder reactions"
Grimblat, N.; Sarotti, A. M.*
Org. Biomol. Chem. 18, 1104-1111 (2020)
doi: 10.1039/C9OB02671A
Grimblat, N.; Sarotti, A. M.*
Org. Biomol. Chem. 18, 1104-1111 (2020)
doi: 10.1039/C9OB02671A
73- "Redefining the impact of Boltzmann analysis in the stereochemical assignment of polar and flexible molecules by NMR calculations"
Zanardi, M. M.; Marcarino, M. O.; Sarotti, A. M.*
Org. Lett. 22, 52-56 (2020)
doi: 10.1021/acs.orglett.9b03866
Zanardi, M. M.; Marcarino, M. O.; Sarotti, A. M.*
Org. Lett. 22, 52-56 (2020)
doi: 10.1021/acs.orglett.9b03866
72- "Total synthesis and structural validation of Phosdiecin A via asymmetric alcohol-mediated carbonyl reductive coupling"
Della-Felice, F.; Sarotti, A. M.; Krische, M. J.*, Pilli, R. A.*
J. Am. Chem. Soc. 141, 13778-13782 (2019)
doi: 10-1021/jacs.9b07512
Della-Felice, F.; Sarotti, A. M.; Krische, M. J.*, Pilli, R. A.*
J. Am. Chem. Soc. 141, 13778-13782 (2019)
doi: 10-1021/jacs.9b07512
71- "Exhaustive exploration of the conformational landscape of mono- and disubstituted five-membered rings by DFT and MP2 calculations"
Stortz, C. A.*; Sarotti, A. M.*
RSC Advances, 9, 24134-24145 (2019)
doi: 10.1039/C9RA03524A
Stortz, C. A.*; Sarotti, A. M.*
RSC Advances, 9, 24134-24145 (2019)
doi: 10.1039/C9RA03524A
70- "Combining the power of J coupling and DP4 analysis on stereochemical assignments: the J-DP4 methods"
Grimblat, N.; Gavin, J. A.; Herández Daranas, A.*; Sarotti, A. M.*
Org. Lett. 21, 4003-4007 (2019).
doi: 10.1021/acs.orglett.9b01193
Grimblat, N.; Gavin, J. A.; Herández Daranas, A.*; Sarotti, A. M.*
Org. Lett. 21, 4003-4007 (2019).
doi: 10.1021/acs.orglett.9b01193
69- "On the effect of intramolecular H-bonding in the configurational assessment of polyhydroxylated compounds with computational methods. The hyacinthacines case"
Zanardi, M. M.; Sortino, M. A.; Sarotti, A. M.*
Carbohydr. Res., 474, 72-79 (2019).
doi: 10.1016/j.carres.2019.01.011
Zanardi, M. M.; Sortino, M. A.; Sarotti, A. M.*
Carbohydr. Res., 474, 72-79 (2019).
doi: 10.1016/j.carres.2019.01.011
68- "An unusual Benzoisoquinoline-9-one derivative and other related compounds with antiproliferative activity from Hawaiian endophytic fungus Peyronellaea sp. FT431"
Li, C.; Sarotti, A. M.; Wu, X.; Yang, B.; Turkson, J.; Chen,. Y.; Liu, Q.; Cao, S.*
Molecules, 24, 196-207 (2019).
doi: 10.3390/molecules24010196
Li, C.; Sarotti, A. M.; Wu, X.; Yang, B.; Turkson, J.; Chen,. Y.; Liu, Q.; Cao, S.*
Molecules, 24, 196-207 (2019).
doi: 10.3390/molecules24010196
67- "Styryl-tetrahydropyran formation by Pd-species: mechanistic insights and structural revision of natural products"
Della-Felice, F.; de Assis, F. F.; Sarotti, A. M.; Pilli, R. A.*
Synthesis, 51, 1545-1560 (2019) - Featured Article
doi: 10.1055/s-0037-1611708
Della-Felice, F.; de Assis, F. F.; Sarotti, A. M.; Pilli, R. A.*
Synthesis, 51, 1545-1560 (2019) - Featured Article
doi: 10.1055/s-0037-1611708
66- "A domino epoxide ring opening-xanthate migration reaction. An alternative entry to thiosugars"
Comba, M. B.; Mangione, M. I.; Suárez, A. G.; Sarotti, A. M.; Spanevello, R. A.*
Eur. J. Org. Chem. 48, 6848-3856 (2018) - Cover Feature of issue 48
doi: 10.1002/ejoc.201801432
Comba, M. B.; Mangione, M. I.; Suárez, A. G.; Sarotti, A. M.; Spanevello, R. A.*
Eur. J. Org. Chem. 48, 6848-3856 (2018) - Cover Feature of issue 48
doi: 10.1002/ejoc.201801432
65- "A general quantum-based NMR method for the assignment of absolute configuration by single or double derivatizations: scope and limitations"
Zanardi, M. M.; Biglione, F. A.; Sortino, M. A.; Sarotti, A. M.*
J. Org. Chem. 83, 11839-11849 (2018)
doi: 10.1021/acs.joc.8b01749
Zanardi, M. M.; Biglione, F. A.; Sortino, M. A.; Sarotti, A. M.*
J. Org. Chem. 83, 11839-11849 (2018)
doi: 10.1021/acs.joc.8b01749
64- "Flabellipparicine, a Flabelliformide-Apparicine-Type bisindole alkaloid from Tabernaemontana divaricata"
Cai, Y. S.; Sarotti, A. M.; Zhou, T. L.; Huang, R.; Qiu, G.; Tian, C.; Miao, Z. H.; Mandi, A.; Kurtan, T.; Cao, S.*; Yang, S. P.*
J. Nat. Prod. 81, 1976-1983 (2018)
doi: 10.1021/acs.jnatprod.8b00191
Cai, Y. S.; Sarotti, A. M.; Zhou, T. L.; Huang, R.; Qiu, G.; Tian, C.; Miao, Z. H.; Mandi, A.; Kurtan, T.; Cao, S.*; Yang, S. P.*
J. Nat. Prod. 81, 1976-1983 (2018)
doi: 10.1021/acs.jnatprod.8b00191
63- "Why lamivudine assmbles into double-stranded helices in crystals: salt heterosynthon versus base-pairing homosynthon"
Capeletti da Silva, C.; Valdo, A. K.; do Nascimento Neto, J. A.; Ribeiro, L.; Sarotti, A. M.; Martins, F. T.*
CrystEngComm, 20, 3049-3057 (2018)
doi: 10.1039/C8CE00100F
Capeletti da Silva, C.; Valdo, A. K.; do Nascimento Neto, J. A.; Ribeiro, L.; Sarotti, A. M.; Martins, F. T.*
CrystEngComm, 20, 3049-3057 (2018)
doi: 10.1039/C8CE00100F
62- "Synthesis of triazole derivatives of levoglucosenone as promising anticancer agents. Effective exploration of the chemical space through retro-aza-Michael//aza-Michael isomerizations"
Tsai, Y. H.; Borini Etichetti, C. M.; Di Benedetto, C.; Girardini, J. E.; Terra-Martins, F., Spanevello, R. A.; Suárez, A. G.; Sarotti, A. M.*
J. Org. Chem. 83, 3516-3528 (2018)
doi: 10.1021/acs.joc.7b03141
Tsai, Y. H.; Borini Etichetti, C. M.; Di Benedetto, C.; Girardini, J. E.; Terra-Martins, F., Spanevello, R. A.; Suárez, A. G.; Sarotti, A. M.*
J. Org. Chem. 83, 3516-3528 (2018)
doi: 10.1021/acs.joc.7b03141
61- "Proton-dependent switching of a novel amino chlorin derivative as fluorescent probe and photosensitizer for acid media"
Heredia, D. A.; Durantini, A. M.; Sarotti, A. M.; Gsponer, N. S.; Ferreyra, D. D.; Bertolini, S. G.; Milanesio, M. E.; Durantini, E. N.*
Chem. Eur. J. 24, 5950-5961 (2018)
doi: 10.1002/chem.201800060
Heredia, D. A.; Durantini, A. M.; Sarotti, A. M.; Gsponer, N. S.; Ferreyra, D. D.; Bertolini, S. G.; Milanesio, M. E.; Durantini, E. N.*
Chem. Eur. J. 24, 5950-5961 (2018)
doi: 10.1002/chem.201800060
60- "NMR and experimental reinvestigation of the condensation reaction between gamma-methylene-alpha,beta-unsaturated aldehydes and propargyl aldehydes"
Riveira, M. J.;* Sarotti, A. M.*
Org. Biomol. Chem. 16, 1442-1447 (2018).
doi: 10.1038/C7OB03110F
Riveira, M. J.;* Sarotti, A. M.*
Org. Biomol. Chem. 16, 1442-1447 (2018).
doi: 10.1038/C7OB03110F
59- "Computer-guided total synthesis of natural products. Recent examples and future perspectives"
Della-Felice, F.; Pilli, R. A.*; Sarotti, A. M.*
J. Braz. Chem. Soc. 29, 1041-1075 (2018).
doi: 10.21577/0103-5053.20180027
Della-Felice, F.; Pilli, R. A.*; Sarotti, A. M.*
J. Braz. Chem. Soc. 29, 1041-1075 (2018).
doi: 10.21577/0103-5053.20180027
58- "Structural revision of two unusual rhamnofolane diterpenes, curcusones I and J, by means of DFT calculations of NMR shifts and coupling constants"
Sarotti, A. M.*
Org. Biomol. Chem. 16, 944-950 (2018).
doi: 10.1039/C7OB02916K
Sarotti, A. M.*
Org. Biomol. Chem. 16, 944-950 (2018).
doi: 10.1039/C7OB02916K
57- "Two new polyketides from Hawaiian endophytic fungus Pestalotiopsis sp. FT172"
Li, C.; Sarotti, A. M.; Yoshida, W.; Cao, S.*
Tetrahedron Lett. 59, 42-45 (2018).
doi: 10.1016/j.tetlet.2017.11.045
Li, C.; Sarotti, A. M.; Yoshida, W.; Cao, S.*
Tetrahedron Lett. 59, 42-45 (2018).
doi: 10.1016/j.tetlet.2017.11.045
56- "Levoglucosenone and its new applications, a way of cellulose residues valorization"
Comba, M. B.; Tsai, Y. H.; Sarotti, A. M.; Mangione, M. I.; Suárez, A. G.; Spanevello, R. A.*
Eur. J. Org. Chem. 5, 590-604 (2018).
doi: 10.1002/ejoc.201701227
Comba, M. B.; Tsai, Y. H.; Sarotti, A. M.; Mangione, M. I.; Suárez, A. G.; Spanevello, R. A.*
Eur. J. Org. Chem. 5, 590-604 (2018).
doi: 10.1002/ejoc.201701227
55- "Probing the competition between acetate and 2,2'-bipyridine ligands to bind to d-block 12 group metals: molecular and structural diversity towards high efficiency luminescent materials".
do Nascimento Neto, J. A.; Capeletti da Silva, C.; Ribeiro, L.; Vasconcelos, G. A.; Vaz, B. G.; Sousa Ferreira, V.; Queiroz Maia, L. K.; Maia, L. J. Q.; Sarotti, A. M.; Terra-Martins, F.*
New J. Chem. 41, 12843-12853 (2017).
doi: 10.1039/C7NJ2393F
do Nascimento Neto, J. A.; Capeletti da Silva, C.; Ribeiro, L.; Vasconcelos, G. A.; Vaz, B. G.; Sousa Ferreira, V.; Queiroz Maia, L. K.; Maia, L. J. Q.; Sarotti, A. M.; Terra-Martins, F.*
New J. Chem. 41, 12843-12853 (2017).
doi: 10.1039/C7NJ2393F
54- "Synthon trends according to acid strenght and geometry in salts of N-heterocyclic bases "
Silva Mendanha Valdo, A. C. Sarotti, A. M.; Terra Martins, F.*
CrystEngComm. 19, 5960-5965 (2017).
doi: 10.1039/C7CE01490B
Silva Mendanha Valdo, A. C. Sarotti, A. M.; Terra Martins, F.*
CrystEngComm. 19, 5960-5965 (2017).
doi: 10.1039/C7CE01490B
53- "Heliotropiumides A and B, new phenolamines with N-carbamoyl putrescine moiety from Heliotropium foertherianum collected in Hawaii and their biological activities"
Caia, Y.; Sarotti, A. M.; Kondratyuk, T. P.; Pezzuto, J. M.; Turkson, J.; Cao, S.*
Bioorg. Med. Chem. Lett. 27, 4630-4634 (2017).
doi: 10.1016/j.bmcl.2017.09.021
Caia, Y.; Sarotti, A. M.; Kondratyuk, T. P.; Pezzuto, J. M.; Turkson, J.; Cao, S.*
Bioorg. Med. Chem. Lett. 27, 4630-4634 (2017).
doi: 10.1016/j.bmcl.2017.09.021
52- "NF-κB inhibitors, unique γ-pyranol-γ-lactams with sulfide and sulfoxide moieties from Hawaiian plant Lycopodiella cernua derived fungus Paraphaeosphaeria neglecta FT462"
Li, C.; Sarotti, A. M.; Huang, P.; Dang, U. T.; Hurdle, J. G.; Kondratyuk, T. P.; Pezzuto, J. M.; Turkson, J.; Cao, S.*
Scientific Reports - Nature. 7, 10424 (2017)
doi: 10.1038/s41598-017-10537-1
Li, C.; Sarotti, A. M.; Huang, P.; Dang, U. T.; Hurdle, J. G.; Kondratyuk, T. P.; Pezzuto, J. M.; Turkson, J.; Cao, S.*
Scientific Reports - Nature. 7, 10424 (2017)
doi: 10.1038/s41598-017-10537-1
51- "Winged-Cone conformation in Hexa-p-tert-butylcalix[6]arene driven by the unusually strong guest encapsulation"
Terra Martins, F.*; de Freitas Oliveira, B. G.; Sarotti, A. M.; de Fátima, A.*
ACS Omega. 2, 5315-5323 (2017).
doi: 10.1021/acsomega.7b00900
Terra Martins, F.*; de Freitas Oliveira, B. G.; Sarotti, A. M.; de Fátima, A.*
ACS Omega. 2, 5315-5323 (2017).
doi: 10.1021/acsomega.7b00900
50- "Catalytic asymmetric synthesis and stereochemical revision of (+)-cryptoconcatone H"
Della-Felice, F.; Sarotti, A. M.; Pilli, R. A.*
J. Org. Chem. 82, 9191-9197 (2017)
doi: 10.1021/acs.joc.7b01378
Della-Felice, F.; Sarotti, A. M.; Pilli, R. A.*
J. Org. Chem. 82, 9191-9197 (2017)
doi: 10.1021/acs.joc.7b01378
49- "A New N-methoxypyridone from the Co-Cultivation of Hawaiian Endophytic Fungi Camporesia sambuci FT1061 and Epicoccum sorghinum FT1062"
Li, C.; Sarotti, A. M.; Yang, B.; Turkson, J.; Cao, S.*
Molecules. 22, 1166-1173 (2017).
doi: 10.3390/molecules22071166
Li, C.; Sarotti, A. M.; Yang, B.; Turkson, J.; Cao, S.*
Molecules. 22, 1166-1173 (2017).
doi: 10.3390/molecules22071166
48- Verbenanone, an octahydro-5H-chromen-5-one from a Hawaiian-plant associated fungus FT431"
Li, C.; Sarotti, A. M.; Turkson, J.; Cao, S.*
Tetrahedron Lett. 58, 2290-2293 (2017).
doi: 10.1016/j.tetlett.2017.04.096
Li, C.; Sarotti, A. M.; Turkson, J.; Cao, S.*
Tetrahedron Lett. 58, 2290-2293 (2017).
doi: 10.1016/j.tetlett.2017.04.096
47- "Sphaerialactonam, a γ-lactam-isochromanone from the Hawaiian endophytic fungus Paraphaesphaeria sp. FT 462"
Huang, P.; Li, C.; Sarotti, A. M.; Turkson, J.; Cao, S.*
Tetrahedron Lett. 58, 1330-1333 (2017).
doi: 10.1016/j.tetlett.2017.02.052
Huang, P.; Li, C.; Sarotti, A. M.; Turkson, J.; Cao, S.*
Tetrahedron Lett. 58, 1330-1333 (2017).
doi: 10.1016/j.tetlett.2017.02.052
46- "Solvatomorphs of 25,26,27,28-tetrahydroxylcalix[4]arene and 5,11,17,23-tetramino-25,26,27,28-tetrabutoxycalix[4]arene: quenching the photoluminiscence through switching the guest"
Terra Martins, F.;* Queiroz Maia, L. J.; da Silva Neto, L.; Moreina da Silva, C.; Sarotti, A. M.; de Fátima, A.*
CrystEngComm. 19, 1792-1800 (2017).
doi: 10.1039/C6CE02649D
Terra Martins, F.;* Queiroz Maia, L. J.; da Silva Neto, L.; Moreina da Silva, C.; Sarotti, A. M.; de Fátima, A.*
CrystEngComm. 19, 1792-1800 (2017).
doi: 10.1039/C6CE02649D
45- "Mechanistic insight into the acid-catalyzed isomerization of biomass-derived polysubstituted pyrrolidines: an experimental and DFT study"
Gerosa, G. G.; Grimblat, N.; Spanevello, R. A.; Suárea, A. G.; Sarotti, A. M.*
Org. Biomol. Chem. 15, 426-434 (2017)
doi: 10.1039/C6OB02457B
Gerosa, G. G.; Grimblat, N.; Spanevello, R. A.; Suárea, A. G.; Sarotti, A. M.*
Org. Biomol. Chem. 15, 426-434 (2017)
doi: 10.1039/C6OB02457B
44- "Determination of the relative configuration of terminal and spiroepoxides by computational methods. Advantages of the inclusion of unscaled data."
Zanardi, M. M.; Suárez, A. G.; Sarotti, A. M.*
J. Org. Chem. 82, 1873-1879 (2017) - Featured Article / ACS Editor´s Choice
doi: 10.1021/acs.joc.6b02129
Zanardi, M. M.; Suárez, A. G.; Sarotti, A. M.*
J. Org. Chem. 82, 1873-1879 (2017) - Featured Article / ACS Editor´s Choice
doi: 10.1021/acs.joc.6b02129
43- "Computational Chemistry Driven Solution to Rubriflordilactone B"
Grimblat, N.; Kaufman, T. S.;* Sarotti, A. M.*
Org. Lett. 18 ,6420–6423 (2016)
doi: 10.1021/acs.orglett.6b03318
Grimblat, N.; Kaufman, T. S.;* Sarotti, A. M.*
Org. Lett. 18 ,6420–6423 (2016)
doi: 10.1021/acs.orglett.6b03318
42- "Experimental and theoretical second harmonic generation and photoluminescence from the pseudo-centrosymmetric dihydrochloride salt dihydrate of trans-1, 2-bis (4-pyridyl) ethene"
Valdo, A. K. S. M.; da Silva, C. C.; Maia, L. J. Q.; Sarotti, A. M.; Martins, F. T.*
CrystEngComm. 19, 346-354 (2017)
doi: 10.1039/C6CE02229D01887D
Valdo, A. K. S. M.; da Silva, C. C.; Maia, L. J. Q.; Sarotti, A. M.; Martins, F. T.*
CrystEngComm. 19, 346-354 (2017)
doi: 10.1039/C6CE02229D01887D
41- "A theoretical study of the Duff reaction: insights into its selectivity"
Grimblat, N.;* Sarotti, A. M.; Kaufman, T. S.; Simonetti, S. O.*
Org. Biomol. Chem. 14, 10496-10501 (2016)
doi: 10.1039/C6OB01887D
Grimblat, N.;* Sarotti, A. M.; Kaufman, T. S.; Simonetti, S. O.*
Org. Biomol. Chem. 14, 10496-10501 (2016)
doi: 10.1039/C6OB01887D
40- "Substituent-Modulated Conformation and Supramolecular Assembly of Tetronamides"
Karak, M.; Acosta, J. A. M.; Barbosa, L. C. A.*; Sarotti, A. M.; da Silva, C. C.; Boukouvalas, J.; Martins, F. T.*
Cryst. Growth Des. 16 , 5798-5810 (2016).
doi: 10.1021/acs.cgd.6b00881
Karak, M.; Acosta, J. A. M.; Barbosa, L. C. A.*; Sarotti, A. M.; da Silva, C. C.; Boukouvalas, J.; Martins, F. T.*
Cryst. Growth Des. 16 , 5798-5810 (2016).
doi: 10.1021/acs.cgd.6b00881
39- "Experimental and theoretical insights in alkenearene intramolecular pi-stacking interaction"
Corne, V.; Sarotti, A. M.; Ramírez de Arellano, C.; Spanevello, R. A.; Suárez, A. G.*
Beilstein J. Org. Chem. 12, 1616-1623 (2016)
doi: 10.3762/bjoc.12.158
Corne, V.; Sarotti, A. M.; Ramírez de Arellano, C.; Spanevello, R. A.; Suárez, A. G.*
Beilstein J. Org. Chem. 12, 1616-1623 (2016)
doi: 10.3762/bjoc.12.158
38- "Thermodynamically driven, syn-selective vinylogous aldol reaction of tetronamides"
Karak, M.; Barbosa, L. C. A.*; Acosta, J. A. M.; Sarotti, A. M.; Boukouvalas, J.
Org. Biomol. Chem. 14, 4897-4907 (2016)
doi: 10.1039/C6OB00895J
Karak, M.; Barbosa, L. C. A.*; Acosta, J. A. M.; Sarotti, A. M.; Boukouvalas, J.
Org. Biomol. Chem. 14, 4897-4907 (2016)
doi: 10.1039/C6OB00895J
37- "Computational chemistry to the rescue: modern toolboxes for the assignment of complex molecules
by GIAO NMR calculations"
Grimblat, N.; Sarotti, A. M.*
Chem. Eur. J. 22, 12246-12261 (2016)
doi: 10.1002/chem.201601150
by GIAO NMR calculations"
Grimblat, N.; Sarotti, A. M.*
Chem. Eur. J. 22, 12246-12261 (2016)
doi: 10.1002/chem.201601150
36- "Synthesis of a thiomannoside"
Comba, M. B.; Suárez, A. G.; Sarotti, A. M.; Mangione, M. I.*; Spanevello, R. A.*; Giordano, E. D. V.
Org. Lett. 18, 1748–1751 (2016)
doi: 10.1021/acs.orglett.6b00428
Comba, M. B.; Suárez, A. G.; Sarotti, A. M.; Mangione, M. I.*; Spanevello, R. A.*; Giordano, E. D. V.
Org. Lett. 18, 1748–1751 (2016)
doi: 10.1021/acs.orglett.6b00428
35- "α-Hydroxyacids accelerate the Diels-Alder reaction of dibutyl vinylboronate with cyclopentadiene:
experimental results and mechanistic insights"
Grimblat, N.; Sarotti, A. M.; Pisano, P. L.; Pellegrinet, S. C.*
New J. Chem. 40, 1966-1969 (2016)
doi: 10.1039/C5NJ03015C
experimental results and mechanistic insights"
Grimblat, N.; Sarotti, A. M.; Pisano, P. L.; Pellegrinet, S. C.*
New J. Chem. 40, 1966-1969 (2016)
doi: 10.1039/C5NJ03015C
34- "Beyond DP4: an improved probability for the stereochemical assignment of isomeric compounds using quantum chemical calculations of NMR shifts"
Grimblat, N.; Zanardi, M. M.; Sarotti, A. M.*
J. Org. Chem. 80, 12526-12534 (2015)
doi: 10.1021/acs.joc.5b02396
Grimblat, N.; Zanardi, M. M.; Sarotti, A. M.*
J. Org. Chem. 80, 12526-12534 (2015)
doi: 10.1021/acs.joc.5b02396
33- "Total synthesis and tentative structural elucidation of Cryptomoscatone E3: interplay of experimental and computational studies"
Novaes, L. F. T.; Sarotti, A. M.; Pilli, R. A.*
J. Org. Chem. 80, 12027-12037 (2015)
doi: 10.1021/acs.joc.5b01956
Novaes, L. F. T.; Sarotti, A. M.; Pilli, R. A.*
J. Org. Chem. 80, 12027-12037 (2015)
doi: 10.1021/acs.joc.5b01956
32- "Cascade cyclization triggered by imine formation. Formal synthesis of the alkaloid (±)-stemoamide and its 9a-epimer"
Brito, G. A.; Sarotti, A. M.; Wipf, P.; Pilli, R. A.*
Tetrahedron Lett. 56, 6664-6668 (2015)
doi: 10.1016/j.tetlet.2015.10.017
Brito, G. A.; Sarotti, A. M.; Wipf, P.; Pilli, R. A.*
Tetrahedron Lett. 56, 6664-6668 (2015)
doi: 10.1016/j.tetlet.2015.10.017
31- "GIAO C-H COSY simulations merged with artificial neural networks pattern recognition analysis. Pushing the structural validation a step forward"
Zanardi, M. M.; Sarotti, A. M.*
J. Org. Chem. 80, 9371-9378 (2015) (Featured Article)
doi: 10.1021/acs.joc.5b01663
Zanardi, M. M.; Sarotti, A. M.*
J. Org. Chem. 80, 9371-9378 (2015) (Featured Article)
doi: 10.1021/acs.joc.5b01663
30- "Understanding reactivity and regioselectivity in Diels-Alder reactions of a sugar-derived dienophile bearing two competing EWGs. An experimental and computational study"
Giri, G. F.; Sarotti, A. M.*; Spanevello, R. A.*
Carbohydr. Res. 415, 54-59 (2015)
doi: 10.1016/j.carres.2014.07.019
Giri, G. F.; Sarotti, A. M.*; Spanevello, R. A.*
Carbohydr. Res. 415, 54-59 (2015)
doi: 10.1016/j.carres.2014.07.019
29- "Joint experimental, in silico and NMR studies towards the rational design of iminium-based organocatalyst derived from renewable sources"
Gerosa, G. G.; Spanevello, R. A.; Suárez, A. G.; Sarotti, A. M.*
J. Org. Chem. 80, 7626-7634 (2015)
doi: 10.1021/acs.joc.5b01214
Gerosa, G. G.; Spanevello, R. A.; Suárez, A. G.; Sarotti, A. M.*
J. Org. Chem. 80, 7626-7634 (2015)
doi: 10.1021/acs.joc.5b01214
28- "Total Synthesis and Structural Elucidation of Cryptolatifolione"
Novaes, L. F. T.; Sarotti, A. M.; Pilli, R. A.*
RSC Advances, 5, 53471-53476 (2015)
doi: 10.1039/C5RA09186A
Novaes, L. F. T.; Sarotti, A. M.; Pilli, R. A.*
RSC Advances, 5, 53471-53476 (2015)
doi: 10.1039/C5RA09186A
27- "Montmorillonite K-10 promoted synthesis of chiral dioxa-caged compounds derived from levoglucosenone"
Zurita, M. A.; Avila, A.; Spanevello, R. A.; Suárez, A. G.; Sarotti, A. M.*
Carbohydr. Res. 402, 67-70 (2015)
doi: 10.1016/j.carres.2014.07.019
Zurita, M. A.; Avila, A.; Spanevello, R. A.; Suárez, A. G.; Sarotti, A. M.*
Carbohydr. Res. 402, 67-70 (2015)
doi: 10.1016/j.carres.2014.07.019
26- "Theoretical insight into the pyrolytic deformylation of levoglucosenone and isolevoglucosenone"
Ariel M. Sarotti*
Carbohydr. Res. 390, 76-80 (2014)
doi: 10.1016/j.carres.2014.03.017
Ariel M. Sarotti*
Carbohydr. Res. 390, 76-80 (2014)
doi: 10.1016/j.carres.2014.03.017
25- "Asymmetric construction of substituted pyrrolidines via 1,3-dipolar cycloaddition of azomethine ylides and chiral acrylates derived from biomass"
Llompart, D. F.; Sarotti, A. M.*; Corne, V.; Suárez, A. G.; Spanevello, R. A.*; Echeverría, G. A.; Piro, O.E.; Castellano, E.E.
Tetrahedron Lett. 55, 2394-2397 (2014)
10.1016/j.tetlet.2014.02.113
Llompart, D. F.; Sarotti, A. M.*; Corne, V.; Suárez, A. G.; Spanevello, R. A.*; Echeverría, G. A.; Piro, O.E.; Castellano, E.E.
Tetrahedron Lett. 55, 2394-2397 (2014)
10.1016/j.tetlet.2014.02.113
24- "Unraveling polar Diels-Alder reactions with conceptual DFT analysis and the distortion/interaction model"
Ariel M. Sarotti*
Org. Biomol. Chem. 12, 187-199 (2014)
doi: 10.1039/C3OB41628C
Ariel M. Sarotti*
Org. Biomol. Chem. 12, 187-199 (2014)
doi: 10.1039/C3OB41628C
23- "Successful combination of computationally inexpensive GIAO 13C NMR calculations and artificial neural network pattern recognition: a new strategy for simple and rapid detection of structural misassignments"
Ariel M. Sarotti*
Org. Biomol. Chem. 11, 4847-4859 (2013)
doi: 10.1039/C3OB40843D
Ariel M. Sarotti*
Org. Biomol. Chem. 11, 4847-4859 (2013)
doi: 10.1039/C3OB40843D
22- "Cellulose recycling as a source of raw chirality"
Valeria Corne, María Celeste Botta, Enrique D. V. Giordano, Germán F. Giri, David F. Llompart, Hernán D. Biava, Ariel M. Sarotti, María I. Mangione, Ernesto G. Mata, Alejandra G. Suárez, Rolando A. Spanevello*
Pure Appl. Chem. 85, 1683-1692 (2013)
doi: 10.1021/ol3008588
Valeria Corne, María Celeste Botta, Enrique D. V. Giordano, Germán F. Giri, David F. Llompart, Hernán D. Biava, Ariel M. Sarotti, María I. Mangione, Ernesto G. Mata, Alejandra G. Suárez, Rolando A. Spanevello*
Pure Appl. Chem. 85, 1683-1692 (2013)
doi: 10.1021/ol3008588
21- "Fuentes alternativas de materia prima"
Rolando A. Spanevello*, Alejandra G. Suárez, Ariel M. Sarotti
Educación Química. 24, 124-131 (2013)
Descargar online
Rolando A. Spanevello*, Alejandra G. Suárez, Ariel M. Sarotti
Educación Química. 24, 124-131 (2013)
Descargar online
20- "Application of the Multi-standard Methodology for Calculating 1H NMR Chemical Shifts"
Ariel M. Sarotti*, Silvina C. Pellegrinet*
J. Org. Chem. 77, 6059–6065 (2012)
doi: 10.1021/jo3008447
Ariel M. Sarotti*, Silvina C. Pellegrinet*
J. Org. Chem. 77, 6059–6065 (2012)
doi: 10.1021/jo3008447
19- "1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides with a Cellulose-Derived Chiral Enone. A Novel Route for Organocatalysts Development"
Ariel M. Sarotti*, Rolando A. Spanevello, Alejandra G. Suárez*, Gustavo A. Echeverría, Oscar E. Piro
Org. Lett. 14, 2556-2559 (2012)
doi: 10.1021/ol3008588
Ariel M. Sarotti*, Rolando A. Spanevello, Alejandra G. Suárez*, Gustavo A. Echeverría, Oscar E. Piro
Org. Lett. 14, 2556-2559 (2012)
doi: 10.1021/ol3008588
18- "Recent Applications of Levoglucosenone as Chiral Synthon"
Ariel M. Sarotti, María M. Zanardi, Rolando A. Spanevello, Alejandra G. Suárez*
Curr. Org. Syn. 9, 439-459 (2012)
doi: 10.2174/157017912802651401
Ariel M. Sarotti, María M. Zanardi, Rolando A. Spanevello, Alejandra G. Suárez*
Curr. Org. Syn. 9, 439-459 (2012)
doi: 10.2174/157017912802651401
17- "Assessing the halogen effect in Diels–Alder reactions involving chiral α-halo enones. A combined experimental and DFT computational approach"
Ariel M. Sarotti*, Rolando A. Spanevello, Alejandra G. Suárez*
Tetrahedron Lett. 52, 4145–4148 (2011)
doi: 10.1016/j.tetlet.2011.05.143
Ariel M. Sarotti*, Rolando A. Spanevello, Alejandra G. Suárez*
Tetrahedron Lett. 52, 4145–4148 (2011)
doi: 10.1016/j.tetlet.2011.05.143
16- "DFT calculations induced a regiochemical outcome revision of the Diels–Alder reaction between levoglucosenone and isoprene"
Ariel M. Sarotti*, Alejandra G. Suárez, Rolando A. Spanevello*
Tetrahedron Lett. 52, 3116–3119 (2011)
doi: 10.1016/j.tetlet.2011.04.021
Ariel M. Sarotti*, Alejandra G. Suárez, Rolando A. Spanevello*
Tetrahedron Lett. 52, 3116–3119 (2011)
doi: 10.1016/j.tetlet.2011.04.021
15- "Experimental and theoretical study of a Diels–Alder reaction between a sugar-derived nitroalkene and cyclopentadiene"
María I. Mangione, Ariel M. Sarotti, Alejandra G. Suárez, Rolando A. Spanevello*
Carbohydr. Res. 346, 460–464 (2011)
doi: 10.1016/j.carres.2010.12.006
María I. Mangione, Ariel M. Sarotti, Alejandra G. Suárez, Rolando A. Spanevello*
Carbohydr. Res. 346, 460–464 (2011)
doi: 10.1016/j.carres.2010.12.006
14- "Evaluation of the use of mandelate derivatives to determine the enantiomeric purity and the absolute configuration of secondary cyclohexenols"
Ariel M. Sarotti, Pablo L. Pisano, Silvina C. Pellegrinet*
Arkivoc (vii), 343-357 (2011)
Descargar online
Ariel M. Sarotti, Pablo L. Pisano, Silvina C. Pellegrinet*
Arkivoc (vii), 343-357 (2011)
Descargar online
13- "Microwave-assisted asymmetric Diels-Alder reaction using chiral auxiliaries derived from biomass"
Ariel M. Sarotti, Rolando A. Spanevello, Alejandra G. Suárez*
Arkivoc (vii), 31-37 (2011)
Descargar online
Ariel M. Sarotti, Rolando A. Spanevello, Alejandra G. Suárez*
Arkivoc (vii), 31-37 (2011)
Descargar online
12- "A facile microwave-assisted Diels–Alder reaction of vinylboronates"
Ariel M. Sarotti, Pablo L. Pisano, Silvina C. Pellegrinet*
Org. Biomol. Chem. 8, 5969-5073 (2010)
doi: 10.1039/C0OB00020E
Ariel M. Sarotti, Pablo L. Pisano, Silvina C. Pellegrinet*
Org. Biomol. Chem. 8, 5969-5073 (2010)
doi: 10.1039/C0OB00020E
11- "A Multi-standard Approach for GIAO 13C NMR Calculations"
Ariel M. Sarotti*, Silvina C. Pellegrinet*
J. Org. Chem. 74, 7254–7260 (2009)
doi: 10.1021/jo901234h
Ariel M. Sarotti*, Silvina C. Pellegrinet*
J. Org. Chem. 74, 7254–7260 (2009)
doi: 10.1021/jo901234h
10- "An experimental/theoretical approach to determine the optical purity and the absolute configuration of endo- and exo-norborn-5-en-2-ol using mandelate derivatives"
Pablo L. Pisano, Ariel M. Sarotti, Silvina C. Pellegrinet*
Tetrahedron Lett. 50, 6121–6125 (2009)
doi: 10.1016/j.tetlet.2009.08.056
Pablo L. Pisano, Ariel M. Sarotti, Silvina C. Pellegrinet*
Tetrahedron Lett. 50, 6121–6125 (2009)
doi: 10.1016/j.tetlet.2009.08.056
9- "Asymmetric Allylboration Reactions with Soderquist’s Chiral 10-Substituted-9-borabicyclo[3.3.2]decanes: A Theoretical Study"
Ariel M. Sarotti, Silvina C. Pellegrinet*
J. Org. Chem. 74, 3562–3565 (2009)
doi: 10.1021/jo900346u
Ariel M. Sarotti, Silvina C. Pellegrinet*
J. Org. Chem. 74, 3562–3565 (2009)
doi: 10.1021/jo900346u
8- "Second generation levoglucosenone-derived chiral auxiliaries. Scope and application in asymmetric Diels–Alder reactions"
Ariel M. Sarotti, Rolando A. Spanevello, Alejandra G. Suárez*
Tetrahedron 65, 3502–3508 (2009)
doi: 10.1016/j.tet.2009.02.020
Ariel M. Sarotti, Rolando A. Spanevello, Alejandra G. Suárez*
Tetrahedron 65, 3502–3508 (2009)
doi: 10.1016/j.tet.2009.02.020
7- "π-Stacking Effect on Levoglucosenone Derived Internal Chiral Auxiliaries. A Case of Complete Enantioselectivity Inversion on the Diels−Alder Reaction"
Ariel M. Sarotti, Israel Fernández, Rolando A. Spanevello, Miguel Á. Sierra*, Alejandra G. Suárez*
Org. Lett. 10, 3389–33924 (2008)
doi: 10.1021/ol801140g
Ariel M. Sarotti, Israel Fernández, Rolando A. Spanevello, Miguel Á. Sierra*, Alejandra G. Suárez*
Org. Lett. 10, 3389–33924 (2008)
doi: 10.1021/ol801140g
6- "An efficient microwave-assisted green transformation of cellulose into levoglucosenone. Advantages of the use of an experimental design approach"
Ariel M. Sarotti, Rolando A. Spanevello, Alejandra G. Suárez*
Green Chem. 9, 1137-1140 (2007)
doi: 10.1039/B703690F
Ariel M. Sarotti, Rolando A. Spanevello, Alejandra G. Suárez*
Green Chem. 9, 1137-1140 (2007)
doi: 10.1039/B703690F
5- "Exploring structural effects of levoglucosenone derived chiral auxiliaries in asymmetric Diels–Alder cycloadditions"
Ariel M. Sarotti, Rolando A. Spanevello, Carine Duhayon, Jean-Pierre Tuchagues, Alejandra G. Suárez*
Tetrahedron 63, 241–251 (2007)
doi: 10.1016/j.tet.2006.10.028
Ariel M. Sarotti, Rolando A. Spanevello, Carine Duhayon, Jean-Pierre Tuchagues, Alejandra G. Suárez*
Tetrahedron 63, 241–251 (2007)
doi: 10.1016/j.tet.2006.10.028
4- "Microwave-Assisted Regioselective Cycloaddition Reactions between 9-Substituted Anthracenes and Levoglucosenone"
Ariel M. Sarotti, Madeleine M. Joullié, Rolando A. Spanevello, Alejandra G. Suárez*
Org. Lett. 8, 5561–5564 (2006)
doi: 10.1021/ol062254g
Ariel M. Sarotti, Madeleine M. Joullié, Rolando A. Spanevello, Alejandra G. Suárez*
Org. Lett. 8, 5561–5564 (2006)
doi: 10.1021/ol062254g
3- "Highly Diastereoselective Diels−Alder Reaction Using a Chiral Auxiliary Derived from Levoglucosenone"
Ariel M. Sarotti, Rolando A. Spanevello, Alejandra G. Suárez*
Org. Lett. 8, 1487–1490 (2006)
doi: 10.1021/ol0603099
Ariel M. Sarotti, Rolando A. Spanevello, Alejandra G. Suárez*
Org. Lett. 8, 1487–1490 (2006)
doi: 10.1021/ol0603099
2- "A chiral auxiliary derived from levoglucosenone in asymmetric Diels–Alder transformations"
Ariel M. Sarotti, Rolando A. Spanevello, Alejandra G. Suárez*
Tetrahedron Lett. 46, 6987–6990 (2005)
doi: 10.1016/j.tetlet.2005.08.073
Ariel M. Sarotti, Rolando A. Spanevello, Alejandra G. Suárez*
Tetrahedron Lett. 46, 6987–6990 (2005)
doi: 10.1016/j.tetlet.2005.08.073
1- "A novel design of a levoglucosenone derived chiral auxiliary"
Ariel M. Sarotti, Rolando A. Spanevello, Alejandra G. Suárez*
Tetrahedron Lett. 45, 8203–8206 (2004)
doi: 10.1016/j.tetlet.2004.09.024
Ariel M. Sarotti, Rolando A. Spanevello, Alejandra G. Suárez*
Tetrahedron Lett. 45, 8203–8206 (2004)
doi: 10.1016/j.tetlet.2004.09.024