syn-diastereoselective carbonyl allylation by 1-or 3-substituted prop-2-en-1-ols with tin(II) iodide and tetrabutylammonium iodide

Citation
Y. Masuyama et al., syn-diastereoselective carbonyl allylation by 1-or 3-substituted prop-2-en-1-ols with tin(II) iodide and tetrabutylammonium iodide, CHEM COMMUN, (13), 1999, pp. 1261-1262
Citations number
8
Language
INGLESE
art.tipo
Article
Categorie Soggetti
Chemistry
Journal title
CHEMICAL COMMUNICATIONS
ISSN journal
1359-7345 → ACNP
Issue
13
Year of publication
1999
Pages
1261 - 1262
Database
ISI
SICI code
1359-7345(19990707):13<1261:SCAB13>2.0.ZU;2-J
Abstract
1-Substituted or 3-substituted prop-2-en-1-ols cause syn-diastereoselective carbonyl allylation with tin(II) iodide and tetrabutylammonium iodide via the formation of 3-substituted prop-2-enylpolyiodotins to produce syn-1,2-d isubstituted but-3-en-1-ols.