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4‐Dimethylaminopyridine‐Catalyzed Regioselective [3+2] Cycloaddition of Isatin‐Derived Morita−Baylis−Hillman Adducts with Azo Esters: A Simple Protocol to Access 3‐Spiropyrazole‐2‐oxindoles
Author(s) -
Ren Yue,
Meng LingGuo,
Peng Tao,
Zhu Lijuan,
Wang Lei
Publication year - 2018
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.201800552
Subject(s) - regioselectivity , chemistry , isatin , cycloaddition , adduct , catalysis , baylis–hillman reaction , combinatorial chemistry , organic chemistry
An efficient and regioselective 4‐dimethylaminopyridine catalyzed [3+2] cycloaddition of isatin‐derived Morita−Baylis−Hillman adducts with azo esters was developed for the construction of 3‐spiropyrazole‐2‐oxindoles. This protocol generated the desired spiropyrazoles in good to excellent yields with good functional group compatibility under mild reaction conditions.