Organic Reactions, Volume 102
John Wiley & Sons, Jul 8, 2020 - Science - 992 pages
The 102nd 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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k CUMULATIVE CHAPTER TITLES BY VOLUME
1,2]-Brook rearrangement acid active acylsilanes added addition afford alcohol aldehydes alkene alkyl alkylidyne Alkyne Conditions Product(s ALKYNE METATHESIS allyl Angew anion aryl bold numbers bond Brook Rearrangement carbanion carbon catalyst CDCl3 charts preceding Chem chromatography complex compound containing Continued corresponding diyne effective efficiency Electrophiles employed epoxide equiv Et2O example followed formation formed functional Fürstner initiates intermediate ketones leads ligands lithium macrocyclic mixture mmol molybdenum n-Bu n-BuLi natural ORGANIC REACTIONS OTBS Ph Ph Ph.Me polymerization preceding the tables preparation presence provides reactive reagents refer Refs resulting ring Scheme silyl solution solvent steps stirred structures indicated substrates synthesis t-Bu Table Takeda TBSO Temp temperature terminal Tetrahedron Lett toluene transformations undergo yield yield Scheme