The Experts below are selected from a list of 180 Experts worldwide ranked by ideXlab platform

S P Petrosyants - One of the best experts on this subject based on the ideXlab platform.

M A Malyarick - One of the best experts on this subject based on the ideXlab platform.

Jimmin Fang - One of the best experts on this subject based on the ideXlab platform.

  • phenyl carbonyl coupling reactions promoted by samarium diiodide and Hexamethylphosphoramide
    Journal of Organic Chemistry, 1997
    Co-Authors: Jiannshyng Shiue, Jimmin Fang
    Abstract:

    By mediation of samarium diiodide and Hexamethylphosphoramide, benzaldehydes and acetophenones underwent self- and cross-couplings to give the products having linkages at the para-carbons of phenyl rings and the carbonyl groups. The phenyl−carbonyl coupling of 2,5-dimethoxybenzaldehyde generated a Sm(III)−enolate intermediate, which was trapped by alkyl halides in a stereospecific manner to give uncommon 1,4-dialkyl-2,5-cyclohexadiene-1-carboxaldehydes. The benzaldehydes bearing tethered carbonyl chains proceeded with intramolecular phenyl−carbonyl couplings to afford fused benzocycles.

  • Phenyl−Carbonyl Coupling Reactions Promoted by Samarium Diiodide and Hexamethylphosphoramide
    Journal of Organic Chemistry, 1997
    Co-Authors: Jiannshyng Shiue, Jimmin Fang
    Abstract:

    By mediation of samarium diiodide and Hexamethylphosphoramide, benzaldehydes and acetophenones underwent self- and cross-couplings to give the products having linkages at the para-carbons of phenyl rings and the carbonyl groups. The phenyl−carbonyl coupling of 2,5-dimethoxybenzaldehyde generated a Sm(III)−enolate intermediate, which was trapped by alkyl halides in a stereospecific manner to give uncommon 1,4-dialkyl-2,5-cyclohexadiene-1-carboxaldehydes. The benzaldehydes bearing tethered carbonyl chains proceeded with intramolecular phenyl−carbonyl couplings to afford fused benzocycles.

  • reductive double electrophilic reactions of methyl thiophenecarboxylate mediated by samarium diiodide and Hexamethylphosphoramide
    Tetrahedron Letters, 1997
    Co-Authors: Shyhming Yang, Jimmin Fang
    Abstract:

    Abstract The pentadienyl anion generated by treating methyl thiophenecarboxylate with samarium diiodide/ Hexamethylphosphoramide in tetrahydrofuran reacts at the C-5 position with a series of benzaldehydes and acetophenones to give the intermediates of samarium dienolates, which are trapped with the second electrophile, such as acetic anhydride, benzyl bromide and carbonyl compounds, in regioselective manners depending on the nature of the electrophile. Thus, the three-component reactions of methyl thiophenecarboxylate with carbonyl compounds are achieved in a one-pot procedure to give 4,5-disubstituted-4,5-dihydrothiophenecarboxylates.

  • samarium diiodide Hexamethylphosphoramide promoted dimerization of benzaldehydes
    Tetrahedron Letters, 1993
    Co-Authors: Jiannshyng Shiue, Jimmin Fang
    Abstract:

    Abstract Benzaldehyde, its ortho - and meta -substituted derivatives and acetophenone underwent dimerization reactions on treatment with samarium(II) iodide in the presence of HMPA. Intramolecular phenyl-carbonyl coupling reactions were similarly carried out.

Lin Pu - One of the best experts on this subject based on the ideXlab platform.

A B Ilyuhin - One of the best experts on this subject based on the ideXlab platform.