3-aryl-1-tetrazol-5-yltriazenes, bench-stable arenediazonium ion synthons: Synthesis of biaryls and aryl halides

Richard N. Butler; Paul D. O'Shea; Declan P. Shelly

doi:10.1039/p19870001039

3-aryl-1-tetrazol-5-yltriazenes, bench-stable arenediazonium ion synthons: Synthesis of biaryls and aryl halides

Richard N. Butler
, Paul D. O'Shea
, Declan P. Shelly

National University of Ireland, Galway

Research output: Contribution to journal › Article › peer-review

11 Citations (Scopus)

Abstract

3-Aryl-1-tetrazol-5-yltriazenes have been used as a bench-stable source of diazonium ions for the synthesis of substituted biaryls, aryl halides (iodides, bromides, and chlorides) and azo dyes. The dediazoniation process when induced by trihalogenoacetic acid or acetic acid did not involve free radicals.

Original language	English
Pages (from-to)	1039-1041
Number of pages	3
Journal	Journal of the Chemical Society, Perkin Transactions 1
DOIs	https://doi.org/10.1039/p19870001039
Publication status	Published - 1987
Externally published	Yes

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10.1039/p19870001039

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title = "3-aryl-1-tetrazol-5-yltriazenes, bench-stable arenediazonium ion synthons: Synthesis of biaryls and aryl halides",

abstract = "3-Aryl-1-tetrazol-5-yltriazenes have been used as a bench-stable source of diazonium ions for the synthesis of substituted biaryls, aryl halides (iodides, bromides, and chlorides) and azo dyes. The dediazoniation process when induced by trihalogenoacetic acid or acetic acid did not involve free radicals.",

author = "Butler, \{Richard N.\} and O'Shea, \{Paul D.\} and Shelly, \{Declan P.\}",

year = "1987",

doi = "10.1039/p19870001039",

language = "English",

pages = "1039--1041",

journal = "Journal of the Chemical Society, Perkin Transactions 1",

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T1 - 3-aryl-1-tetrazol-5-yltriazenes, bench-stable arenediazonium ion synthons

T2 - Synthesis of biaryls and aryl halides

AU - Butler, Richard N.

AU - O'Shea, Paul D.

AU - Shelly, Declan P.

PY - 1987

Y1 - 1987

N2 - 3-Aryl-1-tetrazol-5-yltriazenes have been used as a bench-stable source of diazonium ions for the synthesis of substituted biaryls, aryl halides (iodides, bromides, and chlorides) and azo dyes. The dediazoniation process when induced by trihalogenoacetic acid or acetic acid did not involve free radicals.

AB - 3-Aryl-1-tetrazol-5-yltriazenes have been used as a bench-stable source of diazonium ions for the synthesis of substituted biaryls, aryl halides (iodides, bromides, and chlorides) and azo dyes. The dediazoniation process when induced by trihalogenoacetic acid or acetic acid did not involve free radicals.

UR - https://www.scopus.com/pages/publications/37049081752

U2 - 10.1039/p19870001039

DO - 10.1039/p19870001039

M3 - Article

AN - SCOPUS:37049081752

SN - 1472-7781

SP - 1039

EP - 1041

JO - Journal of the Chemical Society, Perkin Transactions 1

JF - Journal of the Chemical Society, Perkin Transactions 1

ER -

3-aryl-1-tetrazol-5-yltriazenes, bench-stable arenediazonium ion synthons: Synthesis of biaryls and aryl halides

Abstract

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