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Expert Opinion on Therapeutic Patents|March 20, 2014
Modulators of complement activation: a patent review (2008 - 2013)Enrique L Larghi, Teodoro S KaufmanACS Omega|August 9, 2021
Evolution of the Synthesis of Remdesivir. Classical Approaches and Most Recent AdvancesDidier F Vargas, Enrique L Larghi, Teodoro S KaufmanRSC Advances|May 9, 2022
First total synthesis of ampullosine, a unique isoquinoline alkaloid isolated from <i>Sepedonium ampullosporum</i>, and of the related permethylampullosineDidier F Vargas, Enrique L Larghi, Teodoro S KaufmanNatural Product Reports|August 10, 2018
The 6π-azaelectrocyclization of azatrienes. Synthetic applications in natural products, bioactive heterocycles, and related fieldsDidier F Vargas, Enrique L Larghi, Teodoro S KaufmanOrganic & Biomolecular Chemistry|May 1, 2014
A facile and convenient sequential homobimetallic catalytic approach towards β-methylstyrenes. A one-pot Stille cross-coupling/isomerization strategySebastián O Simonetti, Enrique L Larghi, Teodoro S KaufmanThe Journal of Organic Chemistry|March 24, 2022
Total Synthesis of Aqabamycin G, a Nitrophenyl Indolylmaleimide Marine Alkaloid from <i>Vibrio sp</i>. WMBADidier F Vargas, Teodoro S Kaufman, Enrique L LarghiNatural Product Reports|October 8, 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 productsSebastian O Simonetti, Enrique L Larghi, Teodoro S KaufmanOrganic & Biomolecular Chemistry|February 25, 2016
A convenient approach to an advanced intermediate toward the naturally occurring, bioactive 6-substituted 5-hydroxy-4-aryl-1H-quinolin-2-onesSebastián O Simonetti, Enrique L Larghi, Teodoro S KaufmanOrganic & Biomolecular Chemistry|June 17, 2025
Isolation, synthesis and bioactivity of the cassiarins and related compounds: technological applications of polycyclic cassiarinoidsDidier F Vargas, Enrique L Larghi, Teodoro S KaufmanEuropean Journal of Medicinal Chemistry|July 28, 2012
Synthesis and classical pathway Complement inhibitory activity of C7-functionalized filifolinol derivatives, inspired in K-76 COOHEnrique L Larghi, María A Operto, Rene Torres, et al.Pageof 3