The photochemistry of 1-alkenyl-substituted-1,2,3-benzotriazoles leading to formation of indole and fused indole derivatives

9Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Abstract

Under photolysis conditions involving irradiation with a 16 W low pressure mercury arc-lamp (254 nm) or sunlight, functionally substituted 1-vinylbenzotriazoles react efficiently to produce 2-acylindoles, 2-benzotriazol-1-yl-4-methylquinolin-3-ol, isatin, indolo[2,1-b]quinazoline-6, 12-dione (tryptanthrin) and dihydropyrazolo[4,3-b]indole. © ARKAT-USA, Inc.

Cite

CITATION STYLE

APA

Al-Jalal, N., Al-Awadi, N. A., Ibrahim, M. R., & Elnagdi, M. H. (2011). The photochemistry of 1-alkenyl-substituted-1,2,3-benzotriazoles leading to formation of indole and fused indole derivatives. Arkivoc, 2011(10), 288–297. https://doi.org/10.3998/ark.5550190.0012.a24

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free