Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Panjab Arde"'
Autor:
Ramasamy Vijaya Anand, Panjab Arde
Publikováno v:
Organic & Biomolecular Chemistry. 14:5550-5554
A convenient organocatalytic approach to access unsymmetrical diaryl- and triarylmethyl phosphonates using NHC as a Brønsted base catalyst is described. This atom-economical protocol enables the installation of phosphonate groups on p-quinone methid
Autor:
Ramasamy Vijaya Anand, Panjab Arde
Publikováno v:
RSC Advances. 6:77111-77115
The utility of N-heterocyclic carbene as a Bronsted base catalyst for the synthesis of functionalised unsymmetrical triarylmethanes from 2-naphthol and para-quinone methides is described. This protocol allows the installation of naphthyl substituents
Publikováno v:
RSC Adv.. 4:49775-49779
An organo-catalytic protocol for the trimethylsilylation of terminal alkynes employing Ruppert's reagent (CF3SiMe3) as a trimethylsilyl source has been developed under solvent and fluoride free conditions. This method was found to be very effective a
Autor:
Panjab Arde, Ramasamy Vijaya Anand
Publikováno v:
ChemInform. 47
Publikováno v:
Chemistry - An Asian Journal. 8:1489-1496
A combination of the oxidative N-heterocyclic carbene catalysis and click chemistry has been explored for the direct, one-pot synthesis of 1,2,3-triazole derivatives from aromatic aldehydes. This procedure was found to be very efficient and a variety
Publikováno v:
ChemInform. 46
High yields of the products (III), (V), (VII), low catalyst loading, less reaction time, and simple workup are the prominent features of the introduced methodology.
Publikováno v:
ChemInform. 44
A combination of the oxidative N-heterocyclic carbene catalysis and click chemistry has been explored for the direct, one-pot synthesis of 1,2,3-triazole derivatives from aromatic aldehydes. This procedure was found to be very efficient and a variety
Publikováno v:
ChemInform. 43
Publikováno v:
Organicbiomolecular chemistry. 10(4)
The organocatalytic behavior of N-heterocyclic carbenes in the aerobic oxidation of aromatic aldehydes to esters with boronic acids has been explored. This transition metal-free protocol allows access to a wide variety of aromatic esters in good to e