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Alkylation of Nucleophilic Carbon Enolates and Enamines
Polar Addition and Elimination Reactions
24 other sections not shown
acetic acylation adduct alcohols aldehydes aldol condensations alkenes alkynes allylic amides amines anion anti aromatic aryl boron bromide carbanions CARBON NUCLEOPHILES carbonyl compounds carbonyl group carboxylic acids catalyst cation CH3 CH3 CHAPTER 2 REACTIONS Chem chiral chloride conjugate addition converted cyclic cycloaddition deprotonation derivatives double bond E. J. Corey electron elimination ENAMINES enantiomerically enantioselective entry epoxides esters examples formation formed functional groups give Grignard reagents H. C. Brown halides halogen hydride hydroboration hydrogen hydroxyl imine intermediate intramolecular iodide ketones kinetic lithium mechanism mechanistic metal method methyl mixture molecules nucleophilic substitution OCH3 organoboranes organometallic oxidation oxygen prepared procedures proton radical react reaction conditions REACTIONS INVOLVING REACTIONS OF CARBON reactive rearrangement reduction regioselectivity ring salts Scheme SECTION sodium solvents stability starting material step stereochemistry stereoselectivity steric structure syn addition Synth synthesis synthetic Tetrahedron Lett transition ylides