Synthesis of enantiomerically pure isotopomers of 2-phenylpropionic acids

A series of enantiomerically pure [D,13C]‐labeled isotopomeric 2‐phenylpropionic acids were efficiently synthesized using a diastereoselective alkylation and kinetic resolution strategy. Chirality, 2007. © 2007 Wiley‐Liss, Inc.

Saved in:

Bibliographic Details
Published in:	Chirality (New York, N.Y.) Vol. 19; no. 5; pp. 366 - 373
Main Authors:	Chavda, Sameer, Coumbarides, Gregory S., Dingjan, Marco, Eames, Jason, Flinn, Anthony, Ghilagaber, Stephanos, Northen, Julian, Yohannes, Yonas
Format:	Journal Article
Language:	English
Published:	Hoboken Wiley Subscription Services, Inc., A Wiley Company 15-05-2007
Subjects:	2-phenylpropionic acid alkylation chiral diastereoselective evans isotopomers kinetic resolution oxazolidinones profens
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

Description
Summary:	A series of enantiomerically pure [D,13C]‐labeled isotopomeric 2‐phenylpropionic acids were efficiently synthesized using a diastereoselective alkylation and kinetic resolution strategy. Chirality, 2007. © 2007 Wiley‐Liss, Inc.
Bibliography:	ark:/67375/WNG-K9NLX5R4-8 istex:B604F7988CD657A714861E2F4FA8CF8E1EA3C832 ArticleID:CHIR20384 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23
ISSN:	0899-0042 1520-636X
DOI:	10.1002/chir.20384