Abstract:
Direct aminocarbonylation of β-nitroalkenes bearing β-positioned ethoxycarbonyl group using carbamoylsilane as an amide source afforded β-nitro amide derivatives under mild conditions without use of catalysts.
Citation:
Ya. Liu, Yu. Han, J. Chen, “Efficient synthesis of β-nitro amides by aminocarbonylation of ethoxycarbonyl-containing nitroalkenes with carbamoylsilane”, Mendeleev Commun., 31:1 (2021), 128–129
Linking options:
https://www.mathnet.ru/eng/mendc857
https://www.mathnet.ru/eng/mendc/v31/i1/p128
This publication is cited in the following 2 articles:
Chong Tian, Qi Sun, Junfeng Wang, Qiao Chen, Zhiguo Wen, Maxim Borzov, Wanli Nie, “E-Stereospecific 1,1-Carboboration of Terminal Arylalkynes with [IB(C6F5)3]–”, Chinese Journal of Organic Chemistry, 43:1 (2023), 338
Li Junfei, Han Yuling, Liu Yanhong, Chen Jianxin, “Synthesis of β-Nitroamide Derivatives Based on Carbamoylsilane”, Chinese Journal of Organic Chemistry, 42:11 (2022), 3880
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