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Regioselectivity in nucleophilic ring-opening of aziridinones

M. M., Yusoff and Talaty, Erach R. (1998) Regioselectivity in nucleophilic ring-opening of aziridinones. Chemical Communications (9). 985-986 . ISSN 1359-7345 (print), 1364-548X (online)

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Abstract

The proportions of products derived from competing modes of ring-opening of 1,3-di-tert-butylaziridinone and similar aziridinones by a variety of nitrogen, oxygen, sulfur and halogen nucleophiles do not agree with simple guidelines postulated in the literature for these types of aziridinones.

Item Type: Article
Additional Information: 6 Citation. Impact Factor 6.378. Indexed by JCR, Scopus
Subjects: Q Science > Q Science (General)
Q Science > QD Chemistry
Faculty/Division: Faculty of Industrial Sciences And Technology
Depositing User: Prof. Dr. Mashitah Mohd Yusoff
Date Deposited: 05 Mar 2014 03:36
Last Modified: 22 Jan 2018 01:40
URI: http://umpir.ump.edu.my/id/eprint/4771
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