On the mechanism of the reduction of 1-phenyl-3-(4-pyridinylmethylene)-2-oxindole with sodium borohydride in methanol-Reference-Cited by-同舟云学术

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On the mechanism of the reduction of 1-phenyl-3-(4-pyridinylmethylene)-2-oxindole with sodium borohydride in methanol

Published:1994-01 Issue:1 Volume:31 Page:17-23
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:

Author:

Pierce Michael E.,Huhn George F.,Jensen James H.,Sigvardson Ken W.,Islam Qamrul,Xing Yide

Publisher

Wiley

Subject

Organic Chemistry

Reference33 articles.

1. DuP 996 (3,3-bis(4-pyrindinylmethyl)-1-phenylindolin-2-one) enhances the stimulus-induced release of acetylcholine from rat brain in vitro and in vivo

2. Protection against hypoxia-induced passive avoidance deficits: Interactions between DUP 996 and ketanserin

3. W. M. Bryant and G. F. Huhn, U. S. Patent 4806651, (1989)

4. Chem. Abstr., 111, 57536u (1990).

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. Fullerene-Catalyzed Reduction of Azo Derivatives in Water under UV Irradiation;Chemistry - An Asian Journal;2012-09-27

2. 2-Fluoro-4-pyridinylmethyl Analogues of Linopirdine as Orally Active Acetylcholine Release-Enhancing Agents with Good Efficacy and Duration of Action;Journal of Medicinal Chemistry;1998-10-10

3. Metal hydride mediated reduction of 3-(alkylthio)oxindoles containing other potentially reducible groups;Canadian Journal of Chemistry;1997-05-01

4. Acetylcholine release enhancers related to linopirdine: A structure—activity relationship study. II;European Journal of Medicinal Chemistry;1996-01

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