Mechanism of the Fischer indole synthesis. Quantum-chemical interpretation of the rearrangement of substituted cyclohexanone arylhydrazones to tetrahydrocarbazoles-Reference-Cited by-同舟云学术

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Mechanism of the Fischer indole synthesis. Quantum-chemical interpretation of the rearrangement of substituted cyclohexanone arylhydrazones to tetrahydrocarbazoles

Published:1986-07 Issue:7 Volume:22 Page:713-722
ISSN:0009-3122
Container-title:Chemistry of Heterocyclic Compounds
language:en
Short-container-title:Chem Heterocycl Compd

Author:

Vysotskii Yu. B.,Przheval'skii N. M.,Zemskii B. P.,Grandberg I. I.,Kostromina L. Yu.

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry

Link

http://link.springer.com/content/pdf/10.1007/BF00522729.pdf

Reference41 articles.

1. H. Robinson, Usp. Khim., 40, 1434 (1971).

2. Yu. P. Kitaev and T. V. Troepol'skaya, Khim. Geterotsikl. Soedin., No. 8, 1011 (1978).

3. I. I. Grandberg and V. I. Sorokin, Usp. Khim., 43, 266 (1974).

4. I. I. Grandberg, Zh. Org. Khim., 19, 2439 (1983).

5. B. Robinson, The Fischer Indole Synthesis, Wiley Interscience, New York (1982).

Cited by 3 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. Process Intensification of Continuous Flow Synthesis of Tryptophol;Industrial & Engineering Chemistry Research;2018-02-19

2. Category IIac Cyclizations;Indoles;1996

3. PROGRESS IN THE FISCHER INDOLE REACTION. A REVIEW;Organic Preparations and Procedures International;1993-12

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