FeCl3-catalyzed functionalization of monoterpenes via hydroalkylation of unactivated alkenes

Yadav, J. S. ; Subba Reddy, B. V. ; Narasimhulu, G. ; Purnima, K. V. (2009) FeCl3-catalyzed functionalization of monoterpenes via hydroalkylation of unactivated alkenes Tetrahedron Letters, 50 (42). pp. 5783-5785. ISSN 0040-4039

Full text not available from this repository.

Official URL: http://www.sciencedirect.com/science/article/pii/S...

Related URL: http://dx.doi.org/10.1016/j.tetlet.2009.07.057

Abstract

Monoterpenes such as α-pinene, β-pinene, limonene and isolimonene undergo smooth hydroalkoxylation in the presence of 20 mol % of FeCl3 under mild reaction conditions to produce a wide range of the corresponding ethers in excellent yields and with high selectivity.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Terpenes; Iron(III) Reagents; Hydroalkoxylation; Alcohols
ID Code:59663
Deposited On:07 Sep 2011 05:58
Last Modified:07 Sep 2011 05:58

Repository Staff Only: item control page