ANTI-MARKOVNIKOV OPENING OF TRISUBSTITUTED EPOXY ALCOHOLS - APPLICATION IN THE SYNTHESIS OF 2-METHYL-1,3-DIOLS

Citation
Tk. Chakraborty et S. Dutta, ANTI-MARKOVNIKOV OPENING OF TRISUBSTITUTED EPOXY ALCOHOLS - APPLICATION IN THE SYNTHESIS OF 2-METHYL-1,3-DIOLS, Journal of the Chemical Society. Perkin transactions. I, (9), 1997, pp. 1257-1259
Citations number
15
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
0300922X
Issue
9
Year of publication
1997
Pages
1257 - 1259
Database
ISI
SICI code
0300-922X(1997):9<1257:AOOTEA>2.0.ZU;2-E
Abstract
2-Methyl-1,3-diols are synthesized by regioselectively opening trisubs tituted epoxides, prepared from 2-methylbut-2-en-1-ols at the more sub stituted carbon using Cp2TiCl-cyclohexa-1,4-diene.