Scientific Production Faculty

Absolute configuration assignment of 3-indolylacetate esters



Suárez Castillo, Oscar Rodolfo

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.



Research Product




Related articles

Cascade [1,3]-Sigmatropic Rearrangements of Ketene O,O-Acetals: Kinetic and DFT Level Mechanistic St...

Aromatic Bromination versus Oxidation of Indolylmalonates by Bromine

Conformational studies on indole alkaloids from Flustra foliacea by NMR and molecular modeling

First Total Synthesis of ()-Flustraminol B

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

Configuration, stereodynamics and crystal structure of 3-substituted-2-oxofuro[2,3-b]indoles

Synthesis of Bromoindole Alkaloids from Laurencia brongniartii

Firsttotalsyntheses of dihydroflustramine C and flustramine E, alkaloids from the marine bryozoan Fl...

Reactivity of TpMe2Ir(C2H4)(DMAD) with carboxylic acids. A DFT study on geometrical isomers and stru...

Unimolecular rearrangements of ketene-O,O-acetals and fragmentations occurring in the gas phase