p-Quinonemethide Analog of the CC-1065 and Duocarmycin Alkylation Subunits
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00096a043
Cited by 34 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. C-H activation: a Critical Evaluation of a Published Method and its Application Towards Inherently Chiral Calix[4]arenes;S AFR J CHEM-S-AFR T;2020
2. Exploiting Endogenous Cellular Process to Generate Quinone Methides In Vivo;Current Organic Chemistry;2014-01-31
3. ChemInform Abstract: p-Quinonemethide Analogue of the CC-1065 and Duocarmycin Alkylation Subunits.;ChemInform;2010-08-18
4. Synthesis and cytotoxicity evaluation of novel C7–C7, C7–N3 and N3–N3 dimers of 1-chloromethyl-5-hydroxy-1,2-dihydro-3H-benzo[e]indole (seco-CBI) with pyrrole and imidazole polyamide conjugates;Org. Biomol. Chem.;2003
5. Highly E-Selective and Effective Synthesis of Antiarthritic Drug Candidate S-2474 Using Quinone Methide Derivatives;The Journal of Organic Chemistry;2001-12-07
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