Dichlorocyclopropanation and ring cleavage of bridgehead enol lactones. A stereocontrolled ring expansion sequence
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
1. Applications of the intramolecular Diels-Alder reaction to the formation of strained molecules. Synthesis of bridgehead alkenes
2. Synthesis of bridgehead enol lactones via type 2 intramolecular Diels-Alder cycloaddition. New intermediates for stereocontrolled organic synthesis
3. Halomethyl-Metal Compounds. II. The Preparation of gem-Dihalocyclopropanes by the Reaction of Phenyl(trihalomethyl)mercury Compounds with Olefins1
4. Insecticides. Part I. Crystal structures of 1,1-bis-(p-chlorophenyl)-2,2-dichlorocyclopropane and 1,1-bis-(p-ethoxyphenyl)-2,2-dimethylpropane
5. Synthesis of 1-phenyl-5H-2-benzazepines by ring expansion of 1-phenyl-1,2-dihydroisoquinolines
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1. Efficient Preparation of TMSCCl 2 Br and Its Use in Dichlorocyclopropanation of Electron‐Deficient Alkenes;Chemistry – A European Journal;2016-04-26
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3. Some Synthetic Uses of Halides;PATAI'S Chemistry of Functional Groups;2009-12-15
4. SYNTHESIS AND CLEAVAGE OF LACTONES AND THIOLACTONES. APPLICATIONS IN ORGANIC SYNTHESIS. A REVIEW;Organic Preparations and Procedures International;2007-06
5. A protocol to accomplish ‘homo-Robinson’ annulation: application to the guanacastepene problem;Tetrahedron Letters;2005-05
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