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Tunable Base‐Controlled Regioselective Cascade Reaction of 2‐Mercaptobenzimidazole with Morita–Baylis–Hillman Acetates of Nitroalkenes
Author(s) -
Zhang JiaQiang,
Liu JieJie,
Gu ChunLing,
Wang Dong,
Liu Li
Publication year - 2014
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201402752
Subject(s) - chemistry , regioselectivity , combinatorial chemistry , cascade , base (topology) , cascade reaction , organic chemistry , catalysis , mathematical analysis , mathematics , chromatography
Two series of heterocyclic compounds, thiazolo[3,2‐ a ]benzimidazoles and benzimidazo[2,1‐ b ]‐1,3‐thiazines, were synthesized by the tunable base‐controlled regioselective cascade reaction of 2‐mercaptobenzimidazole with Morita–Baylis–Hillman acetates of nitroalkenes in good yields with high regioselectivities.