Title of article
Enantioselective total synthesis of (−)-ericanone
Author/Authors
Dias، نويسنده , , Luiz C. and Kuroishi، نويسنده , , Paula K. and Polo، نويسنده , , Ellen C. and de Lucca Jr.، نويسنده , , Emيlio C.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2013
Pages
3
From page
980
To page
982
Abstract
The first total synthesis of (−)-ericanone was achieved in 10 steps with a 16% overall yield from p-hydroxybenzaldehyde. Notable features of this stereocontrolled approach include a Keck allylation to install the stereocenter at C3 and a 1,5-anti aldol reaction to install the hydroxyl group at C7.
Keywords
total synthesis , natural product , (?)-Ericanone , aldol reaction , Boron enolate
Journal title
Tetrahedron Letters
Serial Year
2013
Journal title
Tetrahedron Letters
Record number
1883731
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