SEARCH Articles Figures Tables A New Reactive Intermediate The Homoenolate Anion Aldehyde homoenolate equivalent Aldehyde homoenolate synthetic equivalents Aldehydes conjugate homoenolate Allyl anions homoenolate anion equivalent Allyl anions homoenolate equivalents Allylamines homoenolate equivalents Allylic anions homoenolate anion equivalent Allylic anions homoenolate equivalents Anionic rearrangement homoenolate equivalents Anionically Protected Lithium Homoenolate Brook rearrangement homoenolate equivalents Carbonyl compounds 3-iodoreduction, homoenolate generation Carbonyl compounds homoenolates Carbonylation homoenolates Carbonylations, homoenolates Chiral homoenolate Comforth model use of copper homoenolate Copper (II) Homoenolate Cycloheptanones homoenolates Cyclopropane, l-silyloxy-2-carboalkoxyring cleavage via homoenolates Cyclopropane, silyloxycleavage homoenolate precursor Cyclopropanes metal homoenolate reaction Depresosterol use of homoenolates Electron-withdrawing-group homoenolate reaction Enals homoenolate equivalents Enolate anions, homoenolates Enolate anions, homoenolates enol ethers Esters, 1,4-keto homoenolates Esters, 1,6-keto zinc homoenolate Functional group equivalents homoenolates Gorgosterol, demethylsynthesis use of homoenolates Group 4 Metal Homoenolates Homoenol Homoenol Homoenolate Homoenolate Homoenolate Acetal derived Homoenolate Allyl carbamates Homoenolate Aryl coupling Homoenolate Enantioselective generation Homoenolate Heteroatom-substituted allyl anions Homoenolate Reaction with electrophiles Homoenolate acylation Homoenolate additions Homoenolate anion equivalent Homoenolate anions Homoenolate chemistry Homoenolate complexes Homoenolate conjugate addition Homoenolate cyclopropanols Homoenolate equivalents Homoenolate ester Homoenolate ions Homoenolate route Homoenolate synthesis Homoenolate synthons Homoenolate, copper Homoenolates 3-protonation Homoenolates addition reactions Homoenolates anion equivalents Homoenolates chiral Homoenolates conjugate additions Homoenolates dianion equivalents Homoenolates elimination reaction Homoenolates equivalents Homoenolates esters Homoenolates homoaldol’ reaction Homoenolates imidazolium-derived Homoenolates radicals Homoenolates reaction Homoenolates reaction with carbonyl compounds Homoenolates siloxycyclopropanes Homoenolates substitution reactions Homoenolates synthesis Homoenolates synthetic utility Homoenolates tautomerism Homoenolates, catalytic generation Homoenolates, formation Iron (III) Homoenolate Ketone homoenolates Ketones homoenolate equivalents Lanthanide homoenolates Lanthanide homoenolates reactions with carbonyl compounds Lead (IV) Homoenolate Lithiation homoenolate equivalent Lithium homoenolate Lithium homoenolates, functionalized Metal homoenolates Methanesulfonate, trifluorovinyl ester reaction with homoenolates NHC-catalyzed Generation of Homoenolates Natural products homoenolate P-Protonation of Homoenolates Palladium Homoenolate Palladium homoenolates Palladium homoenolates 3-elimination Palladium homoenolates catalysts Palladium homoenolates substitution reactions Pfizer Central Research, Groton, CT, USA 14 Metal Homoenolates Propionaldehyde homoenolates Propionamide, 3-stannyllithiation dianionic homoenolate Protonation of Homoenolates Regioselectivity homoenolate anion equivalents Silver Homoenolate Silver homoenolates Silver homoenolates substitution reactions Silyl homoenolates, synthesis Titanium homoenolate Titanium homoenolates Titanium homoenolates reactions Trichlorotitanium homoenolate Umpolung homoenolates ZINC HOMOENOLATE Zinc Chloride homoenolates Zinc homoenolates Zinc homoenolates acylation Zinc homoenolates allylation Zinc homoenolates cyclopropane synthesis Zinc homoenolates preparation Zinc homoenolates reactions Zinc homoenolates substitution reactions Zinc homoenolates, reactivity Zinc-copper homoenolate