A new strategy for yohimbane synthesis based on a silylamido-cyclohexadienone photoinduced radical cyclization process
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Exploratory studies of .alpha.-silylamino- and .alpha.-silylamido-2,5-cyclohexadien-1-one SET photochemistry. Methodology for synthesis of functionalized hydroisoquinolines
2. Enantioselective methods for chiral cyclohexane ring synthesis
3. Model studies probing the amino-Claisen rearrangement approach to hydroisoquinoline synthesis. Development of methods for stereocontrolled introduction of reserpine E ring type functionality
4. Formal total synthesis of deserpidine demonstrating a versatile amino-Claisen rearrangement/Wenkert cyclization strategy for the preparation of functionalized yohimbane ring systems
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2. Enantioselective Conjugate Additions of α-Amino Radicals via Cooperative Photoredox and Lewis Acid Catalysis;Journal of the American Chemical Society;2015-02-16
3. ChemInform Abstract: A New Strategy for Yohimbane Synthesis Based on a Silylamido- Cyclohexadienone Photoinduced Radical Cyclization Process.;ChemInform;2010-08-20
4. Photocatalysis for the Formation of the C−C Bond;Chemical Reviews;2007-05-27
5. A novel photochemical approach to the synthesis of naphthalene-containing lariat-type crown ethers and an evaluation of their metal cation binding and fluorescence sensing properties;Journal of Photochemistry and Photobiology A: Chemistry;2005-10
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