Accession Number:

ADA277936

Title:

Enolboration. 6. Dicyclohexyliodoborane, a Versatile Reagent for the Stereoselective Synthesis of Either Z or E Enolates from Representative Esters

Descriptive Note:

Technical rept.

Corporate Author:

PURDUE UNIV LAFAYETTE IN DEPT OF CHEMISTRY

Personal Author(s):

Report Date:

1994-03-29

Pagination or Media Count:

21.0

Abstract:

A smooth, rapid, quantitative and highly stereoselective synthesis of either Z or E enolates from representative esters has been achieved with dicyclohexyliodo-borane, Chx2BI, in the presence of a suitable tertiary amine, such as triethylamine or N,N-diisopropylethylamine. A systematic investigation of the enolboration of ethyl propionate and ethyl phenylacetate, as model esters, by the various Chx2BX and B-X-9-BBN reagents X OMs, I, and Br established Chx2BI as the preferred reagent in terms of yield and selectivity. Further study of representative esters RCH2COOR with Chx2BI established that both the steric requirements of the alkyl group R at the alpha-position and the alkoxy group OR play a significant role in controlling the enolate geometry. The steric requirements of the amine R 3N also contribute considerably to the stereoselectivity of the reaction. The present study provides a simple procedure for the synthesis of Z or E enol borinates from representative esters RCH2COOR using the combined stereodirecting effects of the alkyl R and the alkoxy OR groups. These enol borinates are highly reactive with aldehydes at temperatures as low as -78 deg C and are exceptionally stereoselective even at 0 deg C. In this exploratory study, the synthesis of stereoselective enolates from representative esters RCH2COOR using Chx2BIR 3N is discussed, with special emphasis on the effects of the steric requirements of R and ORin controlling the enolate geometry.

Subject Categories:

  • Inorganic Chemistry
  • Organic Chemistry
  • Physical Chemistry

Distribution Statement:

APPROVED FOR PUBLIC RELEASE