Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Felipe A. Servín"'
Autor:
Harold, Cruz, Felipe A, Servín, Gerardo, Aguirre, Sergio, Pérez, Domingo, Madrigal, Daniel, Chávez, Andrew L, Cooksy, Ratnasamy, Somanathan
Publikováno v:
ChiralityREFERENCES. 34(6)
We report herein the synthesis and application of enantiopure C
Autor:
Daniel Chávez, Domingo Madrigal, Ratnasamy Somanathan, Andrew L. Cooksy, Sergio Perez-Sicairos, Harold Cruz, Gerardo Aguirre, Felipe A. Servín
Publikováno v:
Chirality. 30:1036-1044
Herein, we report the synthesis of C2 -symmetric sulfonamides as homogeneous and heterogeneous organocatalysts and their application in the enantioselective conjugate 1,4-Michael addition of carbonylic nucleophiles to β-nitrostyrene. Organocatalysts
Autor:
Harold, Cruz, Felipe A, Servín, Domingo, Madrigal, Daniel, Chávez, Sergio, Perez-Sicairos, Gerardo, Aguirre, Andrew L, Cooksy, Ratnasamy, Somanathan
Publikováno v:
Chirality.
Herein, we report the synthesis of C
Autor:
Felipe A. Servín, José A. Romero, Cecilia Anaya de Parrodi, Ratnasamy Somanathan, Domingo Madrigal, Gerardo Aguirre, Daniel Chávez
Publikováno v:
Tetrahedron Letters. 56:2355-2358
We report the synthesis of novel chiral wedge shaped C2-symmetric 1,3-benzenedisulfonamides as organocatalysts that hydrogen bond to the nitroolefins in the transition state of the Michael addition of carbonylic compounds, mimicking natural enzymes,
Autor:
Ratnasamy Somanathan, Felipe A. Servín, José A. Romero, Daniel Chávez, Gerardo Aguirre, Douglas B. Grotjahn
Publikováno v:
Scopus-Elsevier
Here we report a simple and efficient protocol for selectively diamine protection with Boc using Me3SiCl or SOCl2 as HCl source in “one-pot” procedure. This methodology is extended to 1,2- to 1,8-diamines to obtain the corresponding mono-Boc prot
Autor:
Ratnasamy Somanathan, Andrew L. Cooksy, Angélica Navarrate, Gerardo Aguirre, José A. Romero, Domingo Madrigal, Daniel Chávez, Felipe A. Servín
Publikováno v:
Tetrahedron: Asymmetry. 25:997-1001
An oxygen–chlorine interaction is reported in the transition state of the Michael addition of acetone to nitrostyrene catalyzed by enantioenriched monosulfonamides. The interaction between the oxygen from the nitro group and the chlorine at the ort
Autor:
Miguel Parra-Hake, Jorge Gonzalez, Cecilia Anaya de Parrodi, José A. Romero, Felipe A. Servín, Angélica Navarrete, Daniel Chávez, Ratnasamy Somanathan, Gerardo Aguirre
Publikováno v:
Current Organic Chemistry. 16:2440-2461
Autor:
José A. Romero, Felipe A. Servín, Ratnasamy Somanathan, Cecilia Anaya de Parrodi, Daniel Chávez, Gerardo Aguirre, Domingo Madrigal
Publikováno v:
ChemInform. 46
Novel C2 symmetric 1,3-benzenedisulfonamides are successfully applied as organocatalysts that hydrogen bond to the nitroolefin (I) in the transition state of the Michael addition of carbonyl compounds furnishing products (III) and (V) in excellent yi