The synthesis of ketones from carboxylic acids or their derivatives is an important synthetic
operation whereby CC bond construction and functional group interconversion is achieved …

Well over a decade ago, two reviews were contributed to the Organic Reactions series
covering substitution and conjugate addition reactions in organocopper chemistry. Their …

Arylmagnesiation of Alkynes Catalyzed Cooperatively by Iron and Copper Complexes | Journal
of the American Chemical Society ACS ACS Publications C&EN CAS Find my institution Log …

Carboxylic acids were converted directly in 56–99% yields into methyl, n-butyl, and
isopropyl ketones using excess cyanocuprates R2CuLi· LiCN. A substrate with a …

Conjugate Addition of Lithiated Methyl Pyridines to Enones | The Journal of Organic
Chemistry ACS ACS Publications C&EN CAS Find my institution Log In The Journal of …

[5-Acyl-2-(trimethylsilyl) phenyl] iodonium triflates were prepared for the generation of
benzynes bearing ketone function. Treatment of the iodonium triflates with Bu4NF in CH2Cl2 …

Preliminary communication CONCERNING THE SOLUTION COMPOSITION OF THE
NORMANT REAGENT_ NEW THF SOLUBLE METHYL COPPER(I) COMPLEXES Page 1 c47 …

The reagent prepared from 2 PhMgBr and CuI reacts with allyl and benzyl bromides to give
allylbenzene and diphenylmethane, respectively, in 52 and 62% yields. The yields rise to 82 …

The reactions of magnesium-based cuprates 'R2CuMg'(prepared from 2RMgX+ CuI) with
methyl cinnamate furnish conjugate addition products in 60–82% yields. The mixed cuprates …

Arylcoppermagnesium reagents, prepared from 5ArMgX+ 2.5 CuI,(Ar= 4-CH 3 C 6 H 4, 4-CH
3 OC 6 H 4, 4-ClC 6 H 4, 2-C 4 H 3 S react with one equivalent of phthalic anhydride in ether …