Baylis-Hillman reaction of cyclic enones with arenecarbaldehydes and N-arylidene-4-methylbenzenesulfonamides by Using NAP-MgO

Lakshmi Kantam, M. ; Chakrapani, L. ; Choudary, B. M. (2008) Baylis-Hillman reaction of cyclic enones with arenecarbaldehydes and N-arylidene-4-methylbenzenesulfonamides by Using NAP-MgO Synlett, 13 . pp. 1946-1948. ISSN 0936-5214

Full text not available from this repository.

Official URL: http://www.thieme-connect.com/ejournals/abstract/s...

Related URL: http://dx.doi.org/10.1055/s-2008-1077959

Abstract

Baylis-Hillman reaction of cyclic enones with arene­carbaldehydes and N-arylidene-4-methylbenzenesulfonamides under mild conditions by using nanocrystalline MgO (NAP-MgO) afforded the Baylis-Hillman adducts in moderate to good yields with higher selectivity than the corresponding aldol products.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:Baylis-Hillman Reaction; Cyclic Enones; NAP-Mgo; Heterogeneous; Solid Base
ID Code:86053
Deposited On:07 Mar 2012 13:42
Last Modified:07 Mar 2012 13:54

Repository Staff Only: item control page