Selective brominations in nitrobenzene. A convenient synthesis of 3-brornoquinoline, 4-bromoisoquinoline, and 4-phenyl-5-bromopyrimidine-Reference-Cited by-同舟云学术

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Selective brominations in nitrobenzene. A convenient synthesis of 3-brornoquinoline, 4-bromoisoquinoline, and 4-phenyl-5-bromopyrimidine

Published:1973-06 Issue:3 Volume:10 Page:409-410
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:

Author:

Kress Thomas J.,Costantino Silvio M.

Publisher

Wiley

Subject

Organic Chemistry

Reference7 articles.

1. Studies on the bromination of pyrimidine. A facile synthesis of 5-bromopyrimidine

2. Pyridine hydrochlorides gave a mixture of mono- and dibromination. Pyridazine hydrochloride afforded a small amount of an unstable yellow oil.

3. Syntheses of amino and bromo derivatives of 4-methyl-, 4-t-butyl- and 4-phenyl-pyrimidine

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1. Six-Membered Heterocycles;The Chemistry of Heterocycles;2019

2. Palladium-catalyzed enolate arylation as a key C–C bond-forming reaction for the synthesis of isoquinolines;Organic & Biomolecular Chemistry;2016

3. Quinolines and Isoquinolines;Kirk-Othmer Encyclopedia of Chemical Technology;2015-09-23

4. Isoquinoline;Encyclopedia of Reagents for Organic Synthesis;2013-04-22

5. Six-Membered Heterocycles: Quinoline and Isoquinoline;Modern Heterocyclic Chemistry;2011-07-27

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