Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000131.xml
Synfacts 2006(3): 0197-0197
DOI: 10.1055/s-2006-931926
DOI: 10.1055/s-2006-931926
Synthesis of Natural Products and Potential Drugs
© Georg Thieme Verlag Stuttgart · New York
Synthesis of mGluR2/3 Agonists
L. Tan*, N. Yasuda*, N. Yoshikawa, F. W. Hartner, K. K. Eng, W. R. Leonard, F.-R. Tsay, R. P. Volante, R. D. Tillyer
Merck Research Laboratories, Rahway, USA
Further Information
Publication History
Publication Date:
21 February 2006 (online)
Significance
The target molecule is a constrained glutamic acid analogue that mimics L-glutamate, a major excitory neurotransmitter. Potential applications include schizophrenia, depression, anxiety, addiction, pain, epilepsy and neurodegenerative diseases (Parkinson’s and Alzheimer’s). This short, large-scale synthesis (10 steps, 43% overall) features the creation of a cyclopropane ring by an intramolecular epoxide opening by the enolate of an α-fluoro ester (D → E).