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Citation
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HERO ID
1454181
Reference Type
Journal Article
Title
A new method for the synthesis of chiral beta-branched alpha-amino acids
Author(s)
Spangenberg, T; Schoenfelder, A; Breit, B; Mann, A
Year
2007
Is Peer Reviewed?
1
Journal
Organic Letters
ISSN:
1523-7060
EISSN:
1523-7052
Volume
9
Issue
20
Page Numbers
3881-3884
Language
English
PMID
17803310
DOI
10.1021/ol071305m
Abstract
A new method for the synthesis of chiral beta-branched alpha-amino acids based on a copper-mediated directed allylic substitution reaction with Grignard reagents is reported. This is the first case in which a delta-stereogenic center is controlling the diastereoselectivity of an o-DPPB-directed allylic substitution. Depending on the alkene geometry of the starting material either diastereomer, anti or syn, is accessible with good levels of acyclic stereocontrol.
Tags
IRIS
•
n-Butanol
Database searches
Pubmed
Source – January 2013 (private)
Pubmed - 1/2013
Merged reference set - 1/2013
Excluded (not pertinent)
Not chemical specific
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