Controlling the radical 5-exo-trig cyclization, and selective synthesis of seco-iso-cyclopropylfurano[e]indoline (seco-iso-CFI) and seco-cyclopropylthiophene[e]indoline (seco-CTI) DNA alkylating subunit of the duocarmycins
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
1. Shape-Dependent Catalysis: Insights into the Source of Catalysis for the CC-1065 and Duocarmycin DNA Alkylation Reaction
2. CC-1065 and the Duocarmycins: Understanding their Biological Function through Mechanistic Studies
3. CC-1065 and the duocarmycins: unraveling the keys to a new class of naturally derived DNA alkylating agents.
4. The Duocarmycins: Synthetic and Mechanistic Studies
5. Structure and activity relationship of several novel CC-1065 analogs
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1. Design, synthesis, nuclear localization, and biological activity of a fluorescent duocarmycin analog, HxTfA;Bioorganic & Medicinal Chemistry Letters;2018-05
2. Synthesis and evaluation of duocarmycin SA analogs incorporating the methyl 1,2,8,8a-tetrahydrocyclopropa[c]imidazolo[4,5-e]indol-4-one-6-carboxylate (CImI) alkylation subunit;Bioorganic & Medicinal Chemistry;2016-10
3. A Short Review on the Synthetic Strategies of Duocarmycin Analogs that are Powerful DNA Alkylating Agents;Anti-Cancer Agents in Medicinal Chemistry;2015-05-14
4. Synthetic approaches, functionalization and therapeutic potential of quinazoline and quinazolinone skeletons: The advances continue;European Journal of Medicinal Chemistry;2015-01
5. An efficient synthesis of furano analogs of duocarmycin C1 and C2: seco-iso-cyclopropylfurano[e]indoline-trimethoxyindole and seco-cyclopropylfurano[f]quinoline-trimethoxyindole;Tetrahedron Letters;2014-05
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