Sebastian O. Simonetti
Affiliations: | 2011-2016 | Organic Chemistry | Universidad Nacional de Rosario |
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Parents
Sign in to add mentorTeodoro S. Kaufman | grad student | 2011-2016 | Universidad Nacional de Rosario | |
(Currently Assistant Researcher - CONICET) |
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Publications
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Larghi EL, Bracca ABJ, Simonetti SO, et al. (2023) Recent developments in the total synthesis of natural products using the Ugi multicomponent reactions as the key strategy. Organic & Biomolecular Chemistry |
Thobokholt EN, Simonetti SO, Kaufman TS, et al. (2023) Efficient Buchwald-Hartwig and nitrene-mediated five-membered ring closure approaches to the total synthesis of quindoline. Unexpected direct conversion of a nitro group into a phosphazene. Rsc Advances. 13: 13715-13724 |
Simonetti SO, Kaufman TS, Rasia RM, et al. (2021) Thermal decomposition of hexamethylenetetramine: mechanistic study and identification of reaction intermediates via a computational and NMR approach. Organic & Biomolecular Chemistry. 19: 7374-7378 |
Méndez MV, Simonetti SO, Kaufman TS, et al. (2019) A concise Friedländer/Buchwald–Hartwig approach to the total synthesis of quindoline, a bioactive natural indoloquinoline alkaloid, and toward the unnatural 10-methylquindoline New Journal of Chemistry. 43: 10803-10813 |
Grimblat N, Sarotti AM, Kaufman TS, et al. (2016) A theoretical study of the Duff reaction: insights into its selectivity. Organic & Biomolecular Chemistry. 14: 10496-10501 |
Simonetti SO, Larghi EL, Kaufman TS. (2016) The 3,4-dioxygenated 5-hydroxy-4-aryl-quinolin-2(1H)-one alkaloids. Results of 20 years of research, uncovering a new family of natural products. Natural Product Reports. 33: 1425-1446 |
Simonetti SO, Larghi EL, Kaufman TS. (2016) Correction: A convenient approach to an advanced intermediate toward the naturally occurring, bioactive 6-substituted 5-hydroxy-4-aryl-1H-quinolin-2-ones. Organic & Biomolecular Chemistry |
Simonetti SO, Larghi EL, Kaufman TS. (2016) A convenient approach to an advanced intermediate toward the naturally occurring, bioactive 6-substituted 5-hydroxy-4-aryl-1H-quinolin-2-ones. Organic & Biomolecular Chemistry. 14: 2625-36 |
Calvo NL, Simonetti SO, Maggio RM, et al. (2015) Thermally induced solid-state transformation of cimetidine. A multi-spectroscopic/chemometrics determination of the kinetics of the process and structural elucidation of one of the products as a stable N3-enamino tautomer. Analytica Chimica Acta. 875: 22-32 |
Larghi EL, Bracca AB, Arroyo Aguilar AA, et al. (2015) Neocryptolepine: A Promising Indoloisoquinoline Alkaloid with Interesting Biological Activity. Evaluation of the Drug and its Most Relevant Analogs. Current Topics in Medicinal Chemistry. 15: 1683-707 |