Journal article icon

Journal article

A 2,3-butanedione protected chiral glycine equivalent - A new building block for the stereoselective synthesis of enantiopure N-protected α-amino acids

Abstract:
A new chiral glycine equivalent 7 has been synthesised from glycidol using a chiral memory protocol, and its use in the synthesis of N-Z protected α-amino acids was demonstrated in a series of diasteroselective lithium enolate alkylation reactions and subsequent acid hydrolyses.

Actions


Authors


More by this author
Institution:
University of Oxford
Department:
Oxford, MPLS, Chemistry, Organic Chemistry
Role:
Author
Journal:
Chemical Communications
Volume:
9
Issue:
4
Pages:
468-469
Publication date:
2003-02-21
ISSN:
1359-7345
URN:
uuid:79c324bc-8bf1-4c5b-8b44-7af4c588f340
Source identifiers:
327089
Local pid:
pubs:327089
Language:
English

Terms of use


Metrics


Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP