Total Synthesis of (+)-Azinothricin and (+)-Kettapeptin

Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/68627

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DC Field	Value	Language
dc.contributor.author	Hale, K.	-
dc.contributor.author	Manaviazar, S.	-
dc.contributor.author	George, J.	-
dc.contributor.author	Walters, M.	-
dc.contributor.author	Dalby, S.	-
dc.date.issued	2009	-
dc.identifier.citation	Organic Letters, 2009; 11(3):733-736	-
dc.identifier.issn	1523-7060	-
dc.identifier.issn	1523-7052	-
dc.identifier.uri	http://hdl.handle.net/2440/68627	-
dc.description.abstract	Asymmetric total syntheses of (+)-azinothricin and (+)-kettapeptin have been completed through a common new pathway that exploits a highly chemoselective coupling reaction between the fully elaborated cyclodepsipeptide 5 and the glycal activated esters 3 and 4 at the final stages of both respective syntheses.	-
dc.description.statementofresponsibility	Karl J. Hale, Soraya Manaviazar, Jonathan H. George, Marcus A. Walters, and Stephen M. Dalby	-
dc.language.iso	en	-
dc.publisher	Amer Chemical Soc	-
dc.rights	Copyright © 2009 American Chemical Society	-
dc.source.uri	http://dx.doi.org/10.1021/ol802817t	-
dc.subject	Esters	-
dc.subject	Depsipeptides	-
dc.subject	Peptides	-
dc.subject	Molecular Structure	-
dc.subject	Stereoisomerism	-
dc.title	Total Synthesis of (+)-Azinothricin and (+)-Kettapeptin	-
dc.type	Journal article	-
dc.identifier.doi	10.1021/ol802817t	-
pubs.publication-status	Published	-
dc.identifier.orcid	George, J. [0000-0002-7330-2160]	-
Appears in Collections:	Aurora harvest Chemistry publications

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