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Alkylation of 2-methylpyridine at the methylene group

Alkylation of 2-methylpyridine at the methylene group

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A470667027

Alkylation of 2-methylpyridine at the methylene group

About this item

Full title

Alkylation of 2-methylpyridine at the methylene group

Publisher

Springer

Journal title

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2016-08, Vol.52 (8), p.564

Language

English

Formats

Publication information

Publisher

Springer

More information

Scope and Contents

Contents

The reactivity of the 1-triazolyl- and 1-imidazolyl-substituted methylene groups at position 4 of pyridine ring toward alkyl halides is described. Nitrogen heterocycles attached to the methylene group, as well as a 3-cyano group effectively promoted the alkylation, offering a convenient method for constructing structurally diverse molecules that ma...

Alternative Titles

Full title

Alkylation of 2-methylpyridine at the methylene group

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_gale_infotracmisc_A470667027

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A470667027

Other Identifiers

ISSN

0009-3122

DOI

10.1007/s10593-016-1932-5

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