Title of article
anti-Selective enolboration–aldolization of propanoic acid
Author/Authors
Ramachandran، نويسنده , , P. Veeraraghavan and Chanda، نويسنده , , Prem B. and Otoo، نويسنده , , Barnabas، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2014
Pages
3
From page
1289
To page
1291
Abstract
A systematic examination of enolboration–aldolization of propanoic acid has led to an efficient synthesis of anti-β-hydroxy-α-methyl carboxylic acids in consistently high yields and diastereoselectivities by using B-bromodicyclohexylborane as the enolization reagent and triethylamine as the base.
Keywords
B-Bromodicyclohexylborane , Propanoic acid , Aldolization , Enolboration , ?-Hydroxy-?-methyl carboxylic acids
Journal title
Tetrahedron Letters
Serial Year
2014
Journal title
Tetrahedron Letters
Record number
1888196
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