Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Mamillapalli Kishor"'
Publikováno v:
European Journal of Organic Chemistry. 2008:975-993
Here we report on our studies of the use of combinations of amino acids, amines, K2CO3 or Cs2CO3 and CuSO4/Cu for catalysing green cascade reactions. We aimed to prepare the highly reactive and substituted olefin species 7 and 8, under very mild and
Publikováno v:
Tetrahedron Letters. 47:651-656
A novel and green approach for the two-carbon homologation of aldehydes using amino acid catalysis has been developed and further extended to the generation of pharmaceutically active cyano-esters via four-component reactions in one-pot.
Publikováno v:
ChemInform. 41
A practical two-step synthesis of enantioenriched highly substituted perhydrobenzofuran derivatives (V) and (XI) is presented.
Publikováno v:
Organicbiomolecular chemistry. 8(12)
A practical and sustainable chemical process for the synthesis of highly substituted tetrahydro-isobenzofuran-1,5-diones was achieved for the first time through asymmetric cascade Michael-aldol reaction of 4-hydroxy-3-alkyl-5H-furan-2-ones with alkyl
Publikováno v:
ChemInform. 40
We have developed a new technology called multi-catalysis for the sequential one-pot synthesis of highly functionalized heterocycles. A practical and novel multi-component aniline-, self- and Bronsted acid-catalyzed selective process for the sequenti
Publikováno v:
Organicbiomolecular chemistry. 6(22)
We have developed a new technology called multi-catalysis for the sequential one-pot synthesis of highly functionalized heterocycles. A practical and novel multi-component aniline-, self- and Bronsted acid-catalyzed selective process for the sequenti
Publikováno v:
ChemInform. 39
Here we report on our studies of the use of combinations of amino acids, amines, K2CO3 or Cs2CO3 and CuSO4/Cu for catalysing green cascade reactions. We aimed to prepare the highly reactive and substituted olefin species 7 and 8, under very mild and
Publikováno v:
ChemInform. 37
A new, green, regioselective, one-step, tandem reaction of an aldehyde possessing a non-enolizable carbonyl function with a highly substituted cyclohex-2-enone, under amine catalysis afforded highly substituted phenols or 2-arylidenecyclohexanones, r
Publikováno v:
Organic & Biomolecular Chemistry. 6:4176
A direct amino acid-catalyzed chemo- and enantioselective process for the double cascade synthesis of highly substituted 2-alkyl-cyclopentane-1,3-diones, 2-alkyl-3-methoxy-cyclopent-2-enones and Hajos-Parrish (H-P) ketone analogs is presented via red
Publikováno v:
Organic & Biomolecular Chemistry. 4:1641
Novel, economic and environmentally friendly one-pot three-component Knoevenagel/hydrogenation (K/H) and four-component Knoevenagel/hydrogenation/alkylation (K/H/A) reactions of ketones, CH-acids, dihydropyridines and alkyl halides using proline and