Regioselective synthesis of anilines and β-dibrominated acetamides from N-aryl acetoacetamides mediated by Cu(I) salts
Joint Authors
Zhou, Peng
Tan, Li Quan
Liu, Wei Bing
Chen, Cui
Zhang, Qing
Source
Journal of Saudi Chemical Society
Issue
Vol. 20, Issue 2 (31 Mar. 2016), pp.220-226, 7 p.
Publisher
Publication Date
2016-03-31
Country of Publication
Saudi Arabia
No. of Pages
7
Main Subjects
Abstract EN
A highly regioselective synthetic strategy mediated by Cu(I) salts is presented for the synthesis of anilines and b-dibrominated acetamides from N-aryl acetoacetamides.
A variety of N-aryl acetoacetamides were used in this protocol, and a wide range of polysubstituted anilines and b-dibrominated acetamides were obtained in moderate to good yields.
When employing CuI as the additive in this strategy, anilines are obtained, however, when using CuBr as the partner of CuI under a mild condition, b-dibrominated acetamides are afforded.
American Psychological Association (APA)
Tan, Li Quan& Liu, Wei Bing& Zhou, Peng& Chen, Cui& Zhang, Qing. 2016. Regioselective synthesis of anilines and β-dibrominated acetamides from N-aryl acetoacetamides mediated by Cu(I) salts. Journal of Saudi Chemical Society،Vol. 20, no. 2, pp.220-226.
https://search.emarefa.net/detail/BIM-683868
Modern Language Association (MLA)
Tan, Li Quan…[et al.]. Regioselective synthesis of anilines and β-dibrominated acetamides from N-aryl acetoacetamides mediated by Cu(I) salts. Journal of Saudi Chemical Society Vol. 20, no. 2 (Mar. 2016), pp.220-226.
https://search.emarefa.net/detail/BIM-683868
American Medical Association (AMA)
Tan, Li Quan& Liu, Wei Bing& Zhou, Peng& Chen, Cui& Zhang, Qing. Regioselective synthesis of anilines and β-dibrominated acetamides from N-aryl acetoacetamides mediated by Cu(I) salts. Journal of Saudi Chemical Society. 2016. Vol. 20, no. 2, pp.220-226.
https://search.emarefa.net/detail/BIM-683868
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 225-226
Record ID
BIM-683868