2016
Claudia I. Bautista-Hernández, Reyna E. Cordero-Rivera, Erick A. Zúñiga-Estrada, Nayely Trejo-Carbajal, Myriam Meléndez-Rodríguez, Oscar R. Suárez-Castillo, Maricruz Sánchez-Zavala, Martha S. Morales-Ríos, Pedro Joseph-Nathan. Absolute configuration assignment of oxindole derivatives by vibrational circular dichroism exciton coupling. Tetrahedron: Asymmetry, 2016, 27, 623-638. http://dx.doi.org/10.1016/j.tetasy.2016.06.004
Abstract
A convenient and reliable approach for the absolute configuration assignment of oxindole derivatives 2a?m by vibrational circular dichroism (VCD) measurements and evaluation of the VCD bisignated couplet resulting from the interaction of the C2 and C9 carbonyl groups is presented. The absolute configuration assignments were further tested by 1H NMR measurements and by X-ray diffraction analysis.
Stereochemical assignment of naturally occurring 2,3-epoxy-2-methylbutanoate esters
Regioselective Synthesis of 3-Indolyl(alkoxy)acetates
Total Syntheses of Five Indole Alkaloids from the Marine Bryozoan Flustra foliacea
Unimolecular rearrangements of ketene-O,O-acetals and fragmentations occurring in the gas phase
Conformational studies on indole alkaloids from Flustra foliacea by NMR and molecular modeling
Synthesis of Acetamido(indol-3-yl)propanol Derivatives
13C NMR and crystallographic evidence of push-pull effects in furoindolic ?-enamino esters
Role of lipid peroxidation in biliary obstruction in the rat
Synthesis of Bromoindole Alkaloids from Laurencia brongniartii
The absoluteconfiguration of cuauhtemone and related compounds