Potassium iodide catalyzed reductive dehalogenation of α-halo-ketones using Hantzsch ester diethyl 1,4-dihydro-2,6-dimethylpyridine-3,5-dicarboxylate as reductant-Reference-Cited by-同舟云学术

Potassium iodide catalyzed reductive dehalogenation of α-halo-ketones using Hantzsch ester diethyl 1,4-dihydro-2,6-dimethylpyridine-3,5-dicarboxylate as reductant

Published:2010-08 Issue:8 Volume:21 Page:931-934
ISSN:1001-8417
Container-title:Chinese Chemical Letters
language:en
Short-container-title:Chinese Chemical Letters

Author:

Li Hong Sheng,Li Yi Qun

Publisher

Elsevier BV

Subject

General Chemistry

Reference18 articles.

1. Transient Species in the Stepwise Interconversion of NADH and NAD+

2. A facile one-pot synthesis of N-substituted tetrahydroquinolines

3. Reductions with NADH models. 3. The high reactivity of Hantzsch amides

4. Hydrogenation of olefins using Hantzsch ester catalyzed by palladium on carbon

5. A selective reductive amination of aldehydes by the use of Hantzsch dihydropyridines as reductant

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5. O-alkylation of disodium salt of diethyl 3,4-dihydroxythiophene-2,5-dicarboxylate with 1,2-dichloroethane catalyzed by ionic type phase transfer catalyst and potassium iodide;Korean Journal of Chemical Engineering;2013-12-06