Phosphine-catalyzed enantioselective [3 + 2] cycloadditions of γ-substituted allenoates with ß-perfluoroalkyl enones.
Chem Sci
; 8(6): 4660-4665, 2017 Jun 01.
Article
em En
| MEDLINE
| ID: mdl-28936335
ABSTRACT
The enantioselective construction of densely functionalized cyclopentene bearing contiguous three stereocenters has been a challenging task in organic synthesis. Herein, we present a phoshine-catalyzed highly regio-, diastereo- and enantioselective [3 + 2] cycloaddition of γ-substituted allenoates with ß-perfluoroalkyl enones, delivering a wide range of densely functionalized perfluoroalkylated cyclopentenes with three contiguous chiral stereocenters.
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01-internacional
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MEDLINE
Idioma:
En
Ano de publicação:
2017
Tipo de documento:
Article