A NOVEL AND EFFICIENT ROUTE TO (E)-ALK-1-ENYL BORONIC ACID-DERIVATIVES FROM (E)-1-(TRIMETHYLSILYL)ALK-1-ENES AND A FORMAL SUZUKI-MIYAURA CROSS-COUPLING REACTION STARTING WITH VINYLSILANES

Authors
FARINOLA GM FIANDANESE V MAZZONE L NASO F
Citation
Gm. Farinola et al., A NOVEL AND EFFICIENT ROUTE TO (E)-ALK-1-ENYL BORONIC ACID-DERIVATIVES FROM (E)-1-(TRIMETHYLSILYL)ALK-1-ENES AND A FORMAL SUZUKI-MIYAURA CROSS-COUPLING REACTION STARTING WITH VINYLSILANES, Journal of the Chemical Society, Chemical Communications, (24), 1995, pp. 2523-2524
Citations number
33
Categorie Soggetti
Chemistry
Journal title
Journal of the Chemical Society, Chemical Communications → ACNP
ISSN journal
00224936
Issue
24
Year of publication
1995
Pages
2523 - 2524
Database
ISI
SICI code
0022-4936(1995):24<2523:ANAERT>2.0.ZU;2-L
Abstract
A novel and highly efficient conversion of vinylsilanes into vinyl bor onates is described together with their Suzuki-Miyaura cross-coupling reaction, performed without isolating the intermediate resulting from borodesilylation.