Selective Synthesis by Use of Lewis Acids in the Presence of Organocopper and Related Reagents. New Synthetic Methods (61)
- 1 November 1986
- journal article
- review article
- Published by Wiley in Angewandte Chemie-International Edition
- Vol. 25 (11), 947-959
- https://doi.org/10.1002/anie.198609473
Abstract
No abstract availableKeywords
This publication has 88 references indexed in Scilit:
- Reduction-alkylation with organocopper(I) reagents-alkyl halides : Highly regioselective .ALPHA.-alkylation of .GAMMA.-acetoxy-.ALPHA.,.BETA.-enoates with lithium dibutylcuprate-alkyl halides and difference in the reactivity of electron-deficient olefins with organocopper(I)-Lewis acid reagents.CHEMICAL & PHARMACEUTICAL BULLETIN, 1986
- Highly regio- and stereoselective 1,4-addition reaction of .BETA.-cyclopropyl-.ALPHA.,.BETA.-enones with organocopper(I)-aluminum trichloride.CHEMICAL & PHARMACEUTICAL BULLETIN, 1983
- Reactions of allylsilanes and application to organic synthesisPublished by Walter de Gruyter GmbH ,1982
- Organotitanium reagents in organic synthesis a simple means to adjust reactivity and selectivity of carbanionsPublished by Springer Science and Business Media LLC ,1982
- Lewis acid mediated reactions of organocopper reagents. Entrainment in the conjugate addition to .alpha.,.beta.-unsaturated ketones, esters, and acids via the RCu.cntdot.BF3 systemThe Journal of Organic Chemistry, 1982
- Methyl‐triisopropoxy‐titanium, a highly selective nucleophilic methylating reagent. Preliminary CommunicationHelvetica Chimica Acta, 1980
- Geminale Dialkylierung von Ketonen mit Grignard-Verbindungen und Methyltitan(IV)-chloridenAngewandte Chemie, 1980
- Geminal Dialkylation of Ketones with Grignard Compounds and Methyltitanium(IV) ChloridesAngewandte Chemie-International Edition, 1980
- RCu.BF3. 3. Conjugate addition to previously unreactive substituted enoate esters and enoic acidsJournal of the American Chemical Society, 1978
- A novel class of alkylating reagent, RCu.BF3. Substitution of allyl halides with complete allylic rearrangementJournal of the American Chemical Society, 1977