Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/97700
Title: Gold-catalyzed cycloisomerization of 1,7-diyne benzoates to indeno[1,2-c]azepines and azabicyclo[4.2.0]octa-1(8),5-dines
Authors: Rao, Weidong
Koh, Ming Joo
Kothandaraman, Prasath
Chan, Philip Wai Hong
Keywords: DRNTU::Science::Chemistry::Organic chemistry::Organic synthesis
Issue Date: 2012
Source: Rao, W., Koh, M. J., Kothandaraman, P., & Chan, P. W. H. (2012). Gold-catalyzed cycloisomerization of 1,7-diyne benzoates to indeno[1,2-c]azepines and azabicyclo[4.2.0]octa-1(8),5-dines. Journal of the American Chemical Society, 134(26), 10811-10814.
Series/Report no.: Journal of the American chemical society
Abstract: A synthetic method that relies on Au(I)-catalyzed cycloisomerization reactions of 1,7-diyne benzoates to prepare indeno[1,2-c]azepines and azabicyclo[4.2.0]octa-1(8),5-dines is described.
URI: https://hdl.handle.net/10356/97700
http://hdl.handle.net/10220/11264
DOI: 10.1021/ja304964s
Rights: © 2012 American Chemical Society.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

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