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(2R,1'S,2'R)- and (2S,1'S,2'R)-3-[2-Mono(di,tri)fluoromethylcyclopropyl]alanines and their incorporation into hormaomycin analogues

Authors :
Armin de Meijere
Sergei I. Kozhushkov
Dmitrii S. Yufit
Christian Grosse
Marcel Kaiser
Vitaly A. Raev
Source :
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 2844-2857 (2014)
Publication Year :
2014
Publisher :
Beilstein-Institut, 2014.

Abstract

Efficient and scalable syntheses of enantiomerically pure (2R,1'S,2'R)- and (2S,1'S,2'R)-3-[2-mono(di,tri)fluoromethylcyclopropyl]alanines 9a–c, as well as allo-D-threonine (4) and (2S,3R)-β-methylphenylalanine (3), using the Belokon' approach with (S)- and (R)-2-[(N-benzylprolyl)amino]benzophenone [(S)- and (R)-10] as reusable chiral auxiliaries have been developed. Three new fluoromethyl analogues of the naturally occurring octadepsipeptide hormaomycin (1) with (fluoromethylcyclopropyl)alanine moieties have been synthesized and subjected to preliminary tests of their antibiotic activity.

Details

Language :
English
ISSN :
18605397
Volume :
10
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Beilstein Journal of Organic Chemistry
Publication Type :
Academic Journal
Accession number :
edsdoj.98067659fc24c0a80319c6d1efd5c99
Document Type :
article
Full Text :
https://doi.org/10.3762/bjoc.10.302