674309-51-4Relevant academic research and scientific papers
Influence of Michael acceptor stereochemistry on intramolecular Morita-Baylis-Hillman reactions
Teng, Wen-Dong,Huang, Rui,Kwong, Cathy Kar-Wing,Shi, Min,Toy, Patrick H.
, p. 368 - 371 (2007/10/03)
A study of the effect of Michael acceptor stereochemistry on the efficiency of intramolecular Morita-Baylis-Hillman (MBH) reactions has been performed. The reactions were catalyzed by a phosphine, and the reaction substrates studied were enones containing
The intramolecular Baylis-Hillman reaction: Easy preparation of versatile substrates, facile reactions, and synthetic applications
Yeo, Jung Eun,Yang, Xiuling,Kim, Hee Jin,Koo, Sangho
, p. 236 - 237 (2007/10/03)
We have developed a general and highly efficient method for the preparation of diverse ω-formyl-aα,β-unsaturated carbonyl compounds and optimized the conditions for the intramolecular Baylis-Hillman reactions of these compounds to provide various biologic
