Baskaran, Sundarababu ; Balakumar, Vijayakrishnan ; Aravind, Appu (2004) A highly regio- and chemoselective reductive cleavage of benzylidene acetals with EtAlCl2-Et3SiH Synlett (4). pp. 647-650. ISSN 0936-5214
Full text not available from this repository.
Official URL: https://www.thieme-connect.com/products/ejournals/...
Related URL: http://dx.doi.org/10.1055/s-2004-817752
Abstract
A highly regio- and chemoselective reductive cleavage of benzylidene acetals derived from 1,2- and 1,3-diols was achieved under mild conditions using EtAlCl2-Et3SiH reagent system in good to excellent yields. Labile protecting groups such as N-Boc, N-Cbz and -OTBDMS are found to be stable under the reaction conditions.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Thieme Medical Publishers Inc. |
| Keywords: | Regioselectivity; Chemoselectivity; Reductive Cleavage; Benzylidene Acetal; EtAlCl2; Et3SiH |
| ID Code: | 98554 |
| Deposited On: | 19 Sep 2014 11:49 |
| Last Modified: | 19 Sep 2014 11:49 |
Repository Staff Only: item control page
