Issue 2, 1989
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

The chemistry of N-substituted benzotriazoles. Part 14. Novel routes to secondary and tertiary amines and to N, N-disubstituted hydroxylamines

Alan R. Katritzky,   Konstantina Yannakopoulou,   Ping Lue,   Danuta Rasala  and  Laszlo Urogdi  

Abstract

Tertiary amines of types R4R3CHNR1R2(2), (R2CH2)2NR1(10) and (11), or (R2CH2)3N (12), secondary amines of type (R2CH2)2NH (8), and N, N-disubstituted hydroxylamines of type (R2CH2)2NOH (9), are prepared in high yield by the action of Grignard reagents or sodium borohydride on easily available N, N-dialkyl-N-[benzotriazolylalkyl-(or arylalkyl-)]amines (1) or tris(benzotriazolylmethyl)amine (7), on bis(benzotriazolylmethyl)amines (3), (5), and (6), and on N, N-bis(benzotriazolylmethyl)hydroxylamine (4), respectively.

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Article information

DOI
https://doi.org/10.1039/P19890000225
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1989, 225-233

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The chemistry of N-substituted benzotriazoles. Part 14. Novel routes to secondary and tertiary amines and to N, N-disubstituted hydroxylamines

A. R. Katritzky, K. Yannakopoulou, P. Lue, D. Rasala and L. Urogdi, J. Chem. Soc., Perkin Trans. 1, 1989, 225 DOI: 10.1039/P19890000225

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