Issue 24, 2013

Enantioselective phase-transfer catalytic α-alkylation of 2-methylbenzyl tert-butyl malonates

Abstract

A new asymmetric synthetic method to prepare α,α-dialkylmalonates for the construction of a quaternary carbon center via phase-transfer catalytic (PTC) alkylation has been developed. Enantioselective α-alkylation of 2-methylbenzyl tert-butyl α-methylmalonates under phase-transfer catalytic conditions in the presence of (S,S)-3,4,5-trifluorophenyl-NAS bromide (10) afforded the corresponding α,α-dialkylmalonates in high chemical (up to 99%) and optical yields (up to 91% ee), which were selectively hydrolyzed to malonic monoacids under alkali basic conditions for conversion to versatile chiral intermediates.

Graphical abstract: Enantioselective phase-transfer catalytic α-alkylation of 2-methylbenzyl tert-butyl malonates

Supplementary files

Article information

Article type
Paper
Submitted
08 Mar 2013
Accepted
12 Apr 2013
First published
15 Apr 2013

Org. Biomol. Chem., 2013,11, 4030-4039

Enantioselective phase-transfer catalytic α-alkylation of 2-methylbenzyl tert-butyl malonates

M. W. Ha, S. Hong, C. Park, Y. Park, J. Lee, M. Kim, J. Lee and H. Park, Org. Biomol. Chem., 2013, 11, 4030 DOI: 10.1039/C3OB40481A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements