Chemistry of Pyrrolo[1,2-a]indole- and Pyrido[1,2-a]indole-Based Quinone Methides. Mechanistic Explanations for Differences in Cytostatic/Cytotoxic Properties-Reference-Cited by-同舟云学术

Chemistry of Pyrrolo[1,2-a]indole- and Pyrido[1,2-a]indole-Based Quinone Methides. Mechanistic Explanations for Differences in Cytostatic/Cytotoxic Properties

Published:2007-10-10 Issue:23 Volume:72 Page:8636-8647
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Khdour Omar¹,Skibo Edward B.¹

Affiliation:

1. Department of Chemistry and Biochemistry, Arizona State University, Tempe, Arizona 85287-1604

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo070866o

Reference50 articles.

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2. Studies of extended quinone methides. Design of reductive alkylating agents based on the quinazoline ring system

3. Studies of extended quinone methides. Synthesis and physical studies of purine-like monofunctional and bifunctional imidazo[4,5-g]quinazoline reductive alkylating agents

4. Synthesis and physical studies of azamitosene and iminoazamitosene reductive alkylating agents. Iminoquinone hydrolytic stability, syn/anti isomerization, and electrochemistry

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