Reaktionen an Indolderivaten, XVI. Die autoxydative Indol‐Chinolon‐Umwandlung eines Camptothecin‐Modells-Reference-Cited by-同舟云学术

Reaktionen an Indolderivaten, XVI. Die autoxydative Indol‐Chinolon‐Umwandlung eines Camptothecin‐Modells

Published:1972-07 Issue:7 Volume:105 Page:2120-2125
ISSN:0009-2940
Container-title:Chemische Berichte
language:en
Short-container-title:Chem. Ber.

Author:

Warneke Jochen¹,Winterfeldt Ekkehard¹

Affiliation:

1. Organisch‐Chemischen Institut der Technischen Universität Hannover

Publisher

Wiley

Subject

Inorganic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19721050705

Reference13 articles.

1. Reaktionen an Indolderivaten, XV. Die Borhydridreduktion von Bordifluorid‐β‐Dicarbonylkomplexen

2. Plant Antitumor Agents. I. The Isolation and Structure of Camptothecin, a Novel Alkaloidal Leukemia and Tumor Inhibitor from Camptotheca acuminata1,2

3. SieheM. E.Wall inAbhandlungen der Deutschen Akademie der Wissenschaftenzu Berlin1969 4. Internationales Symposium Biochemie und Physiologie der Alkaloide Halle (Saale) 25.–28. Juni 1969 S. 77.

4. General methods of synthesis of indole alkaloids. VI. Syntheses of dl-corynantheidine and a camptothecin model

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