Enantioselective synthesis of (+)-penostatin E.
J Org Chem
; 79(16): 7512-9, 2014 Aug 15.
Article
em En
| MEDLINE
| ID: mdl-25075759
ABSTRACT
The first enantioselective total synthesis of penostatin E has been accomplished. Two highly efficient and diastereoselective reactions, a Hosomi-Sakurai allylation and an intramolecular Pauson-Khand reaction, were utilized for the construction of the basic carbon framework of the target molecule as the key steps. A late-stage introduction of the side chain and a successful base-promoted elimination reaction afforded an efficient synthetic route to (+)-penostatin E.
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1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Alcenos
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Indenos
Idioma:
En
Revista:
J Org Chem
Ano de publicação:
2014
Tipo de documento:
Article
País de afiliação:
Japão