Nucleophilic substitution of benzotriazolylalkyl chlorides with Grignard reagents: A direct route to benzotriazoloalkyl(hetero) aromatic compounds

A R Katritzky; AAA Abdel-Fattah; D O Tymoshenko; S A Belyakov

doi:10.1055/s-1999-3662

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Nucleophilic substitution of benzotriazolylalkyl chlorides with Grignard reagents: A direct route to benzotriazoloalkyl(hetero) aromatic compounds

Journal article

Peer reviewed

Nucleophilic substitution of benzotriazolylalkyl chlorides with Grignard reagents: A direct route to benzotriazoloalkyl(hetero) aromatic compounds

A R Katritzky, AAA Abdel-Fattah, D O Tymoshenko and S A Belyakov

Synthesis (Stuttgart), Vol.1999(Sup. 1), pp.1437-1440

01/01/1999

DOI: https://doi.org/10.1055/s-1999-3662

Abstract

Chemistry

Chemistry, Organic

Physical Sciences

Science & Technology

Benzotriazolylalkyl chlorides 5 react with (hetero)aromatic Grignard reagents generated from the corresponding halogen derivatives to afford benzotriazoloalkyl(hetero)aromatic compounds 8a-k and 10a-c in good yields.

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Title: Nucleophilic substitution of benzotriazolylalkyl chlorides with Grignard reagents: A direct route to benzotriazoloalkyl(hetero) aromatic compounds
Creators - without role: A R Katritzky
AAA Abdel-Fattah
D O Tymoshenko
S A Belyakov
Publication Details: Synthesis (Stuttgart), Vol.1999(Sup. 1), pp.1437-1440
Publisher: Thieme Medical Publishers
Number of pages: 4
Identifiers: 9937722808331
Academic Unit: King Abdulaziz University
Language: English
Resource Type: Journal article