Total synthesis of an anticancer agent, mucocin. 1. Stereoselective synthesis of the left-half segment
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Highly Efficient Synthesis of the Potent Antitumor Annonaceous Acetogenin (+)-Parviflorin
2. Tandem Oxidative Cyclization with Rhenium Oxide. Total Synthesis of 17,18-bisepi-Goniocin
3. Total Synthesis of the Annonaceous Acetogenin (+)-Asimicin. Development of a New Bidirectional Strategy
4. Total Synthesis of the Annonaceous Acetogenins Asiminocin and Asiminecin by a Bidirectional Approach
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1. Acetogenins from Annonaceae;Progress in the Chemistry of Organic Natural Products 101;2016
2. ChemInform Abstract: Total Synthesis of an Anticancer Agent, Mucocin. Part 1. Stereoselective Synthesis of the Left-Half Segment.;ChemInform;2010-06-16
3. Total Synthesis of Annonaceous Acetogenins Belonging to the Non-Adjacent Bis-THF and Non-Adjacent THF-THP Sub-Classes;Molecules;2010-01-21
4. Synthesis of All Possible Isomers Corresponding to the Proposed Structure of Montanacin E, and Their Antitumor Activity;The Journal of Organic Chemistry;2009-08-21
5. Inverse Temperature Dependence in the Diastereoselective Addition of Grignard Reagents to a Tetrahydrofurfural;Organic Letters;2009-03-27
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