A Convenient Synthesis Of Isopropyl Ethers from Secondary Alcohols
- 1 June 1995
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 25 (11) , 1633-1639
- https://doi.org/10.1080/00397919508015848
Abstract
A convenient synthesis of isopropyl ethers from the corresponding secondary alcohols has been developed, involving acetate formation, conversion to the enol ether via an organotitanium reagent, and subsequent catalytic hydrogenation to the isopropyl ether.Keywords
This publication has 6 references indexed in Scilit:
- Isopropenyl glycosides and congeners as novel classes of glycosyl donors: theme and variationsJournal of the American Chemical Society, 1992
- Methylenation of aldonolactonesTetrahedron, 1991
- Titanium-mediated carbonyl olefinations. 1. Methylenations of carbonyl compounds with dimethyltitanoceneJournal of the American Chemical Society, 1990
- Titanium-mediated methylene-transfer reactions. Direct conversion of esters into vinyl ethersJournal of the American Chemical Society, 1980
- Rapid chromatographic technique for preparative separations with moderate resolutionThe Journal of Organic Chemistry, 1978
- Olefin homologation with titanium methylene compoundsJournal of the American Chemical Society, 1978