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https://hdl.handle.net/10356/101199
Title: | Cobalt-catalyzed ortho-C-H alkylation of 2-arylpyridines via ring-opening of aziridines | Authors: | Gao, Ke Paira, Rupankar Yoshikai, Naohiko |
Keywords: | DRNTU::Science::Chemistry::Organic chemistry | Issue Date: | 2014 | Source: | Gao, K., Paira, R., & Yoshikai, N. (2014). Cobalt-Catalyzed ortho -C-H Alkylation of 2-Arylpyridines via Ring-Opening of Aziridines . Advanced Synthesis & Catalysis, 356(7), 1486-1490. | Series/Report no.: | Advanced synthesis & catalysis | Abstract: | A cobalt–N-heterocyclic carbene catalyst, in combination with neopentylmagnesium bromide, was found to promote ortho-C[BOND]H functionalization of 2-arylpyridines with 1,2-diarylaziridines through ring-opening alkylation. The reaction affords 1,1-diarylethanes bearing 2-amino functional groups in moderate to good yields under mild room-temperature conditions. | URI: | https://hdl.handle.net/10356/101199 http://hdl.handle.net/10220/19713 |
ISSN: | 1615-4150 | DOI: | 10.1002/adsc.201400049 | Schools: | School of Physical and Mathematical Sciences | Rights: | © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. | Fulltext Permission: | none | Fulltext Availability: | No Fulltext |
Appears in Collections: | SPMS Journal Articles |
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