Quantifying the enamine-type nucleophilic reactivity of α-aryl vinyl azides

Chemical Communications 2026 Open access

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Authors: Prabaharan Thiruvengetam, Jan Brossette, Christoph Groß, Hendrik Zipse, Armin R. Ofial
DOI: 10.1039/d6cc00190d
Cited by: 0
References: 36

Abstract

of VA and of further styrenes correlate linearly with DFT-calculated methyl cation affinities, which facilitates the design of styrenes with predictable reactivity.

Fields of Study & Subjects

Chemical Reaction Mechanisms Organic Chemistry Cycloaddition Reactions Chemical Reactions and Mechanisms

Publication details

Journal / source
Chemical Communications
Volume
62
Issue
17
Pages
5041–5045
Publication date
1 January 2026
Language
EN