Absolute configuration assignment of oxindole derivatives by vibrational circular dichroism exciton coupling.
Sánchez Zavala, Maricruz
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.
Artículos relacionados
First Total Synthesis of ()-Flustraminol B
Absolute configuration determination of 2-(2-oxo-3-indolyl)acetamide derivatives
Photochemical rearrangements of highly functionalized longipinene derivatives
Regioselective Synthesis of 3-Indolyl(alkoxy)acetates
Synthesis of Bromoindole Alkaloids from Laurencia brongniartii
Transesterifications mediated by t-BuNH2
Synthesis of Indolylindolines Mediated by tert-BuNH2
Cleavage of alkoxycarbonylprotectinggroups from carbamates by t-BuNH2