Title of article
Diastereocontrolled synthesis of an enantiopure 4,4-disubstituted cyclohex-2-en-ol: a new route to (+)-quebrachamine
Author/Authors
Fujimura، نويسنده , , Takashi and Nakashima، نويسنده , , Hiromi and Sakagami، نويسنده , , Hideki and Taniguchi، نويسنده , , Takahiko and Ogasawara، نويسنده , , Kunio، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2002
Pages
3
From page
97
To page
99
Abstract
A diastereoselective route to an enantiopure 4,4-disubstituted cyclohex-2-en-1-ol has been developed using the synthetic equivalent of chiral 4-hydroxycyclohex-2-en-1-one. Its stereochemistry has been determined by its transformation into the Aspidosperma indole alkaloid (+)-quebrachamine.
Journal title
Tetrahedron Letters
Serial Year
2002
Journal title
Tetrahedron Letters
Record number
1649052
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