Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/85595
Title: Carbene-Catalyzed Reductive Coupling of Nitrobenzyl Bromide and Nitroalkene via the Single-Electron-Transfer (SET) Process and Formal 1,4-Addition
Authors: Wang, Yuhuang
Du, Yu
Huang, Xuan
Wu, Xingxing
Zhang, Yuexia
Yang, Song
Chi, Yonggui Robin
Keywords: Single-Electron-Transfer (SET)
Nitrobenzyl Bromide
Issue Date: 2017
Source: Wang, Y., Du, Y., Huang, X., Wu, X., Zhang, Y., Yang, S., et al. (2017). Carbene-Catalyzed Reductive Coupling of Nitrobenzyl Bromide and Nitroalkene via the Single-Electron-Transfer (SET) Process and Formal 1,4-Addition. Organic Letters, 19(3), 632-635.
Series/Report no.: Organic Letters
Abstract: A carbene-catalyzed reductive 1,4-addition of nitrobenzyl bromides to nitroalkenes is disclosed. The reaction proceeds via a carbene-enabled single-electron-transfer process that generates radicals as key intermediates. The present study expands the potentials of carbene catalysis and offers unusual transformations for common substrates in organic synthesis.
URI: https://hdl.handle.net/10356/85595
http://hdl.handle.net/10220/43776
ISSN: 1523-7060
DOI: 10.1021/acs.orglett.6b03792
Rights: © 2017 American Chemical Society.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

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