Organic Reactions, Volume 101The 101st volume in this series for organic chemists in academia and industry presents critical discussions of widely used organic reactions or particular phases of a reaction. The material is treated from a preparative viewpoint, with emphasis on limitations, interfering influences, effects of structure and the selection of experimental techniques. The work includes tables that contain all possible examples of the reaction under consideration. Detailed procedures illustrate the significant modifications of each method. |
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Contents
Edited by Steven M Weinreb | 3 |
Facially Controlled Cycloadditions | 9 |
CHAPTER PAGE | 17 |
CUMULATIVE CHAPTER TITLES BY VOLUME | 933 |
Gilles Dujardinunivlemans | 953 |
961 | |
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Common terms and phrases
activation addition adduct afford aldehyde alkenes approach asymmetric bearing bold numbers bond catalyst catalyzed chart preceding chiral complex Compounds cyclic CYCLOADDITIONS OF OXADIENES derivatives diastereo diastereoselectivity dienophiles DIHYDROPYRANS BY CYCLOADDITIONS DOMINO REACTIONS INVOLVING effect efficient electron-rich employed enals enamines enantioselective endo endo/exo enol ethers enones equiv ester example facial formation functional geometry heat heterodiene highly i-Pr intramolecular intramolecular IODA IODA reactions IODA reactions involving isomer ketene ketones leading Lewis acid MeCN MeO2 MeO2C neat observed obtained OFOXADIENES Continued ORGANIC REACTIONS OXADIENES ACTIVATED pathway Ph Ph position preceding the tables prepared presence proceed promote reactivity Refe refer reported result Scheme selectivity sequence simple Solvent structures indicated substituent synthesis t-Bu TABLE 13 Temp thermal toluene undergo various vinyl ethers Volume yields