Issue 5, 2014

Catalytic asymmetric direct α-alkylation of amino esters by aldehydes via imine activation

Abstract

Two types of BINOL-related chiral aldehydes were used as organocatalysts for the direct α-functionalization of N-unprotected amino esters. The first chiral aldehyde catalysed α-alkylation of 2-aminomalonates with 3-indolylmethanols via imine activation was reported. Various tryptophan derivatives were produced in good yields and with high enantioselectivities. A reasonable mechanism was proposed and the core intermediates were identified by high resolution mass spectroscopy (HRMS).

Graphical abstract: Catalytic asymmetric direct α-alkylation of amino esters by aldehydes via imine activation

Supplementary files

Article information

Article type
Edge Article
Submitted
03 Dec 2013
Accepted
29 Jan 2014
First published
31 Jan 2014

Chem. Sci., 2014,5, 1988-1991

Catalytic asymmetric direct α-alkylation of amino esters by aldehydes via imine activation

B. Xu, L. Shi, Y. Zhang, Z. Wu, L. Fu, C. Luo, L. Zhang, Y. Peng and Q. Guo, Chem. Sci., 2014, 5, 1988 DOI: 10.1039/C3SC53314J

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