Producción Científica Profesorado

Absolute configuration assignment of 3-indolylacetate esters.



Sánchez Zavala, Maricruz

2012

Vázquez-Arredondo, R. M., Suárez-Castillo, O. R., Meléndez-Rodríguez, M., Sánchez-Zavala, M., Cano-Escudero, I. C., Bautista-Hernández, C. I., Cruz-Borbolla, J., Morales-Ríos, M. S., & Joseph-Nathan, P. (2012). Absolute configuration assignment of 3-indolylacetate esters. Tetrahedron: Asymmetry 23, 1279-1293.


Abstract


Herein we describe a straightforward method for the determination of the absolute configuration of 3-indolyl(bromo)acetate 7, 3-indolyl(alkoxy)acetates 8a?f and 3-indolyl(amino)acetate 8g, based on 1H NMR spectral analysis. The conformational preferences for two diastereomeric esters were calculated by DFT, which matched very well with the experimental results. X-ray diffraction analysis allowed us to validate the methodology, and independent absolute configuration evidence was obtained by vibrational circular dichroism



Producto de Investigación




Artículos relacionados

Quirogane, Prenopsane, and Patzcuarane Skeletons Obtained by Photochemically Induced Molecular Rearr...

Synthesis of Bromoindole Alkaloids from Laurencia brongniartii

Synthesis of Indolylindolines Mediated by tert-BuNH2

Transesterifications mediated by t-BuNH2

Preparation of 3-hydroxyoxindoles with dimethyldioxirane and their use for the synthesis of naturalp...

First Total Synthesis of ()-Flustraminol B

Mechanisticstudies of the photochemicalrearrangement of 1-oxolongipin-2-ene derivatives

DFT and NMR parameterized conformation of valeranone

Photochemical rearrangements of highly functionalized longipinene derivatives

Absolute configuration determination of 2-(2-oxo-3-indolyl)acetamide derivatives