STEREOSELECTIVE SYNTHESIS OF ENOL ACETATES BY THE REACTION OF ALKENYLBORONATES WITH (DIACETOXYIODO)BENZENE AND SODIUM-IODIDE

Citation
M. Murata et al., STEREOSELECTIVE SYNTHESIS OF ENOL ACETATES BY THE REACTION OF ALKENYLBORONATES WITH (DIACETOXYIODO)BENZENE AND SODIUM-IODIDE, Journal of the Chemical Society. Perkin transactions. I, (9), 1998, pp. 1465-1466
Citations number
28
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
0300922X
Issue
9
Year of publication
1998
Pages
1465 - 1466
Database
ISI
SICI code
0300-922X(1998):9<1465:SSOEAB>2.0.ZU;2-Q
Abstract
Stereochemically pure (E)- and (Z)-alk-1-en-1-yl acetates have been ea sily prepared by acetoxylation of the (Z)- and (E)-alk-1-en-1-ylboroni c acids or their esters, respectively, with (diacetoxyiodo)benzene and sodium iodide, in reasonable yields.