Palladium Catalysed Reactions of Baylis-Hillman Products: Synthesis of Some Useful Intermediates
✍ Scribed by Kumareswaran, R.; Vankar, Yashwant D.
- Book ID
- 118053759
- Publisher
- Taylor and Francis Group
- Year
- 1998
- Tongue
- English
- Weight
- 412 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0039-7911
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Acelates derived from a variety of the Baylis-Hillman products undergo reduction with HCOOH in the presence of Et.~N, Pd(OAc)2, and dppe (or tri-isepropylphosphite) to yield the corresponding trisubstituted Z-otefins in good yields displaying high regio and stereoselectivity.
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract A facile, fast and high efficiency micellar EKC has been explored for the analysis and UV detection of __p__‐nitrobenzaldehyde and 2‐[hydroxy(4‐nitrophenyl)methyl]‐2‐cyclopenten‐1‐one with a buffer electrolyte of 30.0 mM tetraborate and 50.0 mM sodium taurodeoxycholate at pH 9.3. Under