1155922-27-2Relevant academic research and scientific papers
Copper-catalyzed domino SN2′/coupling reaction: A versatile and facile synthesis of cyclic compounds from baylis-hillman acetates
Niu, Qingsheng,Mao, Hui,Yuan, Guodong,Gao, Jilong,Liu, Haiquan,Tu, Yawei,Wang, Xiaoxia,Lv, Xin
, p. 1185 - 1192 (2013)
A variety of substituted quinoline/pyridine, thiochromene and naphthalene derivatives, which might be of biological and medicinal value, were synthesized by copper-catalyzed domino SN2′/coupling, SN2′ /deacylation/coupling and SN2′/coupling/elimination reactions. The method provides a general and convenient approach to the synthesis of various substituted cyclic compounds from the corresponding Baylis-Hillman (B-H) acetates and N-/S-/C-nucleophiles. Copyright
Synthesis of poly-substituted tetrahydropyridines from Baylis-Hillman adducts modified with N-allylamino group via radical cyclization
Lee, Hyun Seung,Kim, Eun Sun,Kim, Sung Hwan,Kim, Jae Nyoung
scheme or table, p. 2274 - 2277 (2009/08/07)
An expedient method was developed for the synthesis of 1,4,5,6-tetrahydropyridines by radical cyclization protocol involving consecutive 1,5-hydrogen transfer and double bond isomerization process starting from Baylis-Hillman adducts.
