Indole, 6. Mitt. Lactamisierung von 4,9-Dihydropyrano[3,4-b]indol-1(3H)-onen mit Methylamin. – Ein neuer Syntheseweg zu Strychnocarpin und seinen Derivaten-Reference-Cited by-同舟云学术

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Indole, 6. Mitt. Lactamisierung von 4,9-Dihydropyrano[3,4-b]indol-1(3H)-onen mit Methylamin. – Ein neuer Syntheseweg zu Strychnocarpin und seinen Derivaten

Published:1988 Issue:7 Volume:321 Page:411-414
ISSN:0365-6233
Container-title:Archiv der Pharmazie
language:de
Short-container-title:Arch. Pharm. Pharm. Med. Chem.

Author:

Lehmann Jochen,Pohl Ursula

Publisher

Wiley

Subject

Drug Discovery,Pharmaceutical Science

Reference17 articles.

1. Indole, 5. Mitt.: 4,9-Dihydro-1-methylimino-3H-pyrano[3,4-b]indole aus 4,9-Dihydropyrano[3,4-b]indol-1(3H)-onen

2. Alkaloids from Strychnos floribunda

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3. Facile Synthesis of Indolelactones Using Mn(III)-Based Oxidative Substitution-Cyclization Reaction;HETEROCYCLES;2018

4. N-Heterocyclic Carbene-Catalyzed Enantioselective Annulation of Indolin-3-ones with Bromoenals;Chemistry - An Asian Journal;2014-04-11

5. Synthesis and Biological Evaluation of Novel Tetrahydro-β-carboline Derivatives as Antitumor Growth and Metastasis Agents through Inhibiting the Transforming Growth Factor-β Signaling Pathway;Journal of Medicinal Chemistry;2014-01-27

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