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Conjugate addition of allylic lithium organocuprates and allylic organocopper(I) compounds to α-acetylenic esters

✍ Scribed by Philippe Miginiac; Gérard Daviaud; François Gérard


Publisher
Elsevier Science
Year
1979
Tongue
French
Weight
235 KB
Volume
20
Category
Article
ISSN
0040-4039

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✦ Synopsis


at low temperature, allylic lithium organocuprates and allylic organocopper(1) compounds add stereoselectively (cisaddition)to a-acetylenic esters to afford a,&-biethylenic esters. Lithium organocuprates react at low temperature nit esters to give a-ethylenic esters corresponding to R2CuLi + R'-CK-COOC2H5 V


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✍ Pieter S. van Heerden; Barend C.B. Bezuidenhoudt; Daneel Ferreira 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 192 KB

The organocopper-Lewis acid system, RCu-TMEDA-BuzBOTf, is useful for conjugate addition to highly constrained chiral c~,lS-unsaturated N-acyl imidazolidiannes. In comparison with the corresponding TMSCi-activated reagents, Bu2BOTf exhibits a dramatic increase in reactivity during 1,4-addition of ben