Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/21341
Title: Diastereoselective synthesis of the acyl side-chain and amino acid (2S,3R)-3-hydroxy-3-methylproline fragments of polyoxypeptin A
Authors: Chen, Z
Ye, T 
Keywords: Amino acids
Asymmetric aldol
Asymmetric dihydnoxylation
Homoenolate
Ketone allylation
Polyoxypeptin A
Issue Date: 2005
Publisher: Georg Thieme Verlag
Source: Synlett, 2005, v. , no. 18, w01405st, p. 2781-2785 How to cite?
Journal: Synlett 
Abstract: Synthesis of the acyl side-chain and amino acid (2S,3R)-3-hydroxy-3- methylproline units of the potent depsipeptide polyoxypeptin A, is described. Key intermediates were secured via diastereoselective addition involving a homoenolate ion and allylation of an aminoketone, respectively.
URI: http://hdl.handle.net/10397/21341
ISSN: 0936-5214
EISSN: 1437-2096
DOI: 10.1055/s-2005-918924
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