Visible light triggered photo-decomposition of vinyl azides to (E)-stilbene derivatives via 1,2-acyl migration
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Updated: Jan 23, 2026

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
Published on: April 22, 2016
Satheesh Borra1, Lodsna Borkotoky, Uma Devi Newar
1Applied Organic Chemistry Group, Chemical Sciences & Technology Division, CSIR-North East Institute of Science & Technology (NEIST), Jorhat-785006, Assam, India. ram.cdri@gmail.com.
Abstract:
An efficient photocatalyst-free visible light assisted synthetic route to various (E)-stilbene derivatives was developed. The reaction proceeds through a denitrogenative photo-decomposition of vinyl azides into 2H-azirines followed by neighboring amino group assisted ring opening, 1,2-acyl migration and enolization. The photochemical reaction offers light harvesting without any photocatalyst to access a wide variety of substituted (E)-stilbenes in moderate to high yields.
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