Journal
TETRAHEDRON LETTERS
Volume 50, Issue 43, Pages 5903-5905Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2009.08.004
Keywords
Diethyltartrate; Johnson-Claisen rearrangement; Acute ischemic stroke therapeutic agent; Arundic acid
Categories
Funding
- IRCC
- IIT-Bombay
- CSIR New Delhi
Ask authors/readers for more resources
A diethyltartrate-based synthesis of both enantiomers of the acute ischemic stroke therapeutic agent, arundic acid is presented. Separable diastereomers were obtained through the Johnson-Claisen rearrangement of the chiral vicinal diol based on the diethyltartrate skeleton and were converted separately into the two enantiomers of arundic acid. (C) 2009 Elsevier Ltd. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available