2,3,4,9-Tetrahydro-1H-pyrido[3,4-b]indoles.II. Reversible transformation of 1-alkyl-2-(4,9-dihydro-3H-pyrido[3,4-b]indol-1-yl)cyclohexanol into 1-alkylidene-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indoles
Subject
Organic Chemistry
Reference18 articles.
1. Tris (1,1,1,2,2,3,3-heptafluoro-7,7-dimethyl-d6-4,6-octanedione-d3)-europium III, Merck and Company, Inc.
2. Synthesis of 1-substituted-2,3,4,9-tetrahydro-(2-oxopropyl)-1H-pyrido [3,4-b] indoles and their base-catalyzed rearrangements toN- [2-[2-(1-alkyl-3-oxobutenyl)-1H-indol-3-yl] ethyl]acetamides
3. Anthrachinhydron und Anthrachinhydron‐carbonsäuren
4. R. R. Frazer and Y. Y. Wigfield, Chem. Commun., 1471 (1970).
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. Iridium-Catalysed Asymmetric Hydrogenation of Enamides in the Presence of 3,3′-Substituted H8-Phosphoramidites;Advanced Synthesis & Catalysis;2009-06
2. Synthesis of Enantiomerically Pure 1,2,3,4‐Tetrahydro‐β‐carbolines andN‐Acyl‐1‐aryl Ethylamines by Rhodium‐Catalyzed Hydrogenation;Chemistry – An Asian Journal;2008-07-07
3. ChemInform Abstract: 2,3,4,9-Tetrahydro-1H-pyrido(3,4-b)indoles. Part 2. Reversible Transformation of 1-Alkyl-2-(4,9-dihydro-3H-pyrido(3,4-b)indol-1-yl)cyclohexanol into 1-Alkylidene-2,3,4,9-tetrahydro-1H-pyrido(3,4-b)indoles.;ChemInform;1987-11-17