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- W2564442103 endingPage "6767" @default.
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- W2564442103 abstract "Abstract A mild and convenient method for the synthesis of 4‐arylsulfonylmethyl substituted quinolines has been developed. The manganese(III) acetate mediated reaction of 2‐(2‐alkynylphenyl)aminomaleates, via free‐radical sulfonylation, 6‐endo‐trig cyclization and aromatization, produced 4‐arylsulfonylmethylquinolines with good functional group tolerance. This arylsulfonylation‐cyclization reaction could also proceed with a sequential one‐pot method. The use of inexpensive, readily available KMnO 4 and p ‐toluenesulfinic acid sodium salts makes this protocol very efficient and practical." @default.
- W2564442103 created "2017-01-06" @default.
- W2564442103 creator A5001224100 @default.
- W2564442103 creator A5013468442 @default.
- W2564442103 creator A5045594996 @default.
- W2564442103 creator A5064685908 @default.
- W2564442103 date "2016-12-16" @default.
- W2564442103 modified "2023-10-16" @default.
- W2564442103 title "Manganese Salts Mediated Free-Radical Arylsulfonation-Cyclization of 2-(2-Alkynylphenyl)aminomaleates" @default.
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