61752-53-2Relevant academic research and scientific papers
d5-Reactions of Doubly Deprotonated γ,δ-Unsaturated Carbonyl Derivatives with Electrophiles. A Novel Approach to the Synthesis of Tetrahydrofuran and Tetrahydropyran Derivatives
Seebach, Dieter,Pohmakotr, Manat,Schregenberger, Christian,Weidmann, Beat,Mali, Raghao S.,Pohmakotr, Srisuke
, p. 419 - 450 (2007/10/02)
The dienone-dianion derivatives 1 react with all types of electrophiles tested (alkyl halide, silyl chloride, ester, ketone, aldehyde, epoxide) to give β,υ-unsaturated carbonyl compounds of type A (see Formulae 2-6, 13, 14 and Tables 1-5).The α- and β-hyd
GENERATION OF DIENONE AND TRIENONE DIANION DERIVATIVES; DOUBLE DEPROTONATION AS A ROUTE TO LUMO-FILLED ?-SYSTEMS
Seebach, Dieter,Pohmakotr, Manat
, p. 4047 - 4058 (2007/10/02)
Conjugated unsaturated carbonyl compounds and their analogues 1 are a1,3,5...-reagents.An umpolung of this intrinsic reactivity can be achieved by generation of the dianions 2, LUMO filled ?-systems, from hydrogenated precursors, see schemes 1
