A New Stereocontrolled Synthetic Route to (-)-Echinosporin from D-Glucose via Padwa Allenylsulfone [3+2]-Anionic Cycloadditive Elimination


Autoria(s): Flasz, Jakub T; Hale, Karl J
Data(s)

15/06/2012

Resumo

A new formal total synthesis of (-)-echinosporin has been developed based upon the Padwa [3 + 2]-cycloadditive elimination reaction of allenylsulfone 4 with the D-glucose-derived enone 14 which provides cycloadduct 12.

Identificador

http://pure.qub.ac.uk/portal/en/publications/a-new-stereocontrolled-synthetic-route-to-echinosporin-from-dglucose-via-padwa-allenylsulfone-32anionic-cycloadditive-elimination(d4774079-2821-4aea-bd66-29f53686fa87).html

http://dx.doi.org/10.1021/ol301090v

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Flasz , J T & Hale , K J 2012 , ' A New Stereocontrolled Synthetic Route to (-)-Echinosporin from D-Glucose via Padwa Allenylsulfone [3+2]-Anionic Cycloadditive Elimination ' Organic Letters , vol 14 , no. 12 , pp. 3024-3027 . DOI: 10.1021/ol301090v

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