Reaction of organozinc halides with aryl isocyanates
H Yang, D Huang, KH Wang, C Xu, T Niu, Y Hu
Index: Yang, Haoran; Huang, Danfeng; Wang, Ke-Hu; Xu, Changming; Niu, Teng; Hu, Yulai Tetrahedron, 2013 , vol. 69, # 12 p. 2588 - 2593
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Citation Number: 5
Abstract
Reformatsky reagent, benzylzinc bromide or alkylzinc iodides react with aryl isocyanates directly to give corresponding N-substituted carbamates under mild reaction conditions. However, the reaction of allylzinc bromide or propargylzinc bromide with aryl isocyanates produces the corresponding N-substituted amides. The reactions provide alternative methods for the synthesis of N-substituted carbamates or amides.
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