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


Autoria(s): Hale, Karl J; Manaviazar, Soraya; George, J.H.; Walters, M.A.; Dalby, S.M.
Data(s)

05/02/2009

Resumo

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.

Identificador

http://pure.qub.ac.uk/portal/en/publications/total-synthesis-of-azinothricin-and-kettapeptin(712bd10d-f472-4ade-a860-b16cd7e9cf79).html

http://dx.doi.org/10.1021/ol802817t

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Hale , K J , Manaviazar , S , George , J H , Walters , M A & Dalby , S M 2009 , ' Total Synthesis of (+)-Azinothricin and (+)-Kettapeptin ' Organic Letters , vol 11 , no. 3 , pp. 733-736 . DOI: 10.1021/ol802817t

Palavras-Chave #/dk/atira/pure/subjectarea/asjc/1600/1605 #Organic Chemistry #/dk/atira/pure/subjectarea/asjc/1600/1606 #Physical and Theoretical Chemistry #/dk/atira/pure/subjectarea/asjc/1300/1303 #Biochemistry
Tipo

article