Radical reaction of the dimethacrylic ester of (2R,4R)-2,4-pentanediol. Addition-cyclization-termination process of high yield under rigorous stereocontrol of the termination step
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference4 articles.
1. Rotamer distribution control and double Michael addition for cyclopentane annulation with superb selectivity
2. Stereochemistry of Radical Reaction;Curran,1996
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1. ChemInform Abstract: Radical Reaction of the Dimethacrylic Ester of (2R,4R)-2,4-Pentanediol. Addition-Cyclization-Termination Process of High Yield under Rigorous Stereocontrol of the Termination Step.;ChemInform;2010-08-03
2. Stereocontrol in Radical Cyclization: Change in Rate-Determining Step;Organic Letters;2010-07-21
3. Stereoselective Formation of a Chiral Ether by Intramolecular O–H Insertion Reaction of a Metal Carbenoid Generated from Diazoacetoacetate;European Journal of Organic Chemistry;2008-01
4. Carbanion vs. Carbon Radical in Tandem 1,4-Addition to Two Connected Units of Acrylate or Methacrylate;Bulletin of the Chemical Society of Japan;2007-10-15
5. Thiophenol;Encyclopedia of Reagents for Organic Synthesis;2006-09-15
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