Issue 0, 1987
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

The chemistry of N-substituted benzotriazoles. Part 1.1-(Chloromethyl)benzotriazole

Alan R. Katritzky,   Stanislaw Rachwal,   Kenneth C. Caster,   Fatma Mahni,   Kam Wah Law  and  Olga Rubio  

Abstract

The N-chloromethyl group of 1-(chloromethyl)benzotriazole undergoes nucleophilic substitution by carbon, nitrogen, phosphorus, oxygen, and sulphur nucleophiles. α-Lithiation was achieved in high yield in 1-phenylthiomethyl-, 1-phenylsulphinylmethyl-, and 1-(phenylstilphonylmethyl)benzotriazoles and the lithio derivatives reacted with a variety of electrophiles. New benzotriazolium salts were prepared by quaternization of the N-3 nitrogen with methyl iodide.

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Article information

DOI
https://doi.org/10.1039/P19870000781
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1987, 781-789

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The chemistry of N-substituted benzotriazoles. Part 1.1-(Chloromethyl)benzotriazole

A. R. Katritzky, S. Rachwal, K. C. Caster, F. Mahni, K. W. Law and O. Rubio, J. Chem. Soc., Perkin Trans. 1, 1987, 781 DOI: 10.1039/P19870000781

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