Chemoselective aminomethylation of bifunctional substrates: carbonyl versus phenolic hydroxyl, carbonyl versus pyrazole and pyrrole versus phenolic hydroxyl as competing activating groups-Reference-Cited by-同舟云学术

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Chemoselective aminomethylation of bifunctional substrates: carbonyl versus phenolic hydroxyl, carbonyl versus pyrazole and pyrrole versus phenolic hydroxyl as competing activating groups

Published:2014-02 Issue:6 Volume:55 Page:1229-1233
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Roman Gheorghe

Funder

European Union’s Seventh Framework Programme

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference47 articles.

1. Mannich Bases: Chemistry and Uses;Tramontini,1994

2. The Merck Index,2001

3. Further advances in the chemistry of mannich bases

4. Advances in the Chemistry of Mannich Bases

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. BRIEF EXAMINATION OF THE ANTIMICROBIAL ACTIVITY OF PHENOLIC MANNICH BASES DERIVED FROM BUTYLATED HYDROXYANISOLE;FARMACIA;2019-12-20

2. 2-Naphthol-pyrazole conjugates as substrates in the Mannich reaction;Zeitschrift für Naturforschung B;2018-03-20

3. Aminomethylation of substituted pyrroles and 4,5,6,7-tetrahydroindoles with biogenic cyclic amines;Russian Journal of Organic Chemistry;2017-02

4. ChemInform Abstract: Chemoselective Aminomethylation of Bifunctional Substrates: Carbonyl versus Phenolic Hydroxyl, Carbonyl versus Pyrazole and Pyrrole versus Phenolic Hydroxyl as Competing Activating Groups.;ChemInform;2014-06-26

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