Pachamuthu, Kandaswamy ; Vankar, Yashwant D. (1998) Palladium catalysed regio and stereoselective reduction of Baylis-Hillman coupling products derived allylic acetates Tetrahedron Letters, 39 (30). pp. 5439-5442. 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/S0040-4039(98)01049-1
Abstract
Acetates derived from a variety of the Baylis-Hillman products undergo reduction with HCOOH in the presence of Et3N, Pd(OAc)2, and dppe (or tri-isopropylphosphite) to yield the corresponding trisubstituted Z-olefins in good yields displaying high regio and stereoselectivity.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| ID Code: | 58195 |
| Deposited On: | 31 Aug 2011 06:36 |
| Last Modified: | 31 Aug 2011 06:36 |
Repository Staff Only: item control page
