Zobrazeno 1 - 10
of 22
pro vyhledávání: '"B. Madhu Babu"'
Publikováno v:
Synlett. 27:631-639
A novel synthesis of bisheteroarylaryl methanes and triarylmethanes is described by the selective C–C bond cleavage of acetophenones in the presence of SeO2/lanthanide chlorides. The present strategy provides an in situ generation of aldehydes from
Publikováno v:
Tetrahedron Letters. 56:1775-1779
An efficient and general protocol is described for the synthesis of bisindolylmethanes by the reaction of indole with aldehydes in the presence of BF3·OEt2. The method is rapid and applicable for aromatic, heteroaromatic, and aliphatic aldehydes.
Publikováno v:
Tetrahedron Letters. 56:766-771
An efficient, convenient, and novel one pot approach is described for the synthesis of triarylmethanes by in situ oxidation of benzylalcohols followed by the Friedel–Crafts alkylation of di/trimethoxybenzenes in the presence of BF 3 ·OEt 2 . The g
Publikováno v:
Tetrahedron Letters. 55:3473-3477
A mild and novel approach is described for the synthesis of functionalized fused imidazole analogues in solvent-free and catalyst-free condition in ionic liquid. The short reaction time, good isolated yields, generality and environmentally benign rea
Publikováno v:
Tetrahedron Letters. 55:1868-1872
A rapid, efficient, and convenient synthesis of functionalized triarylmethane is described by the Friedel–Crafts alkylation of methoxybenzenes with a variety of aldehydes in the presence of BF 3 ·OEt 2 . The generality of the method is demonstrate
Autor:
Harshadas M. Meshram, Vikas M. Bangade, Pramod B. Thakur, B. Chennakesava Reddy, B. Madhu Babu
Publikováno v:
Tetrahedron Letters. 54:4767-4771
An efficient regioselective synthesis of 3-aryl imidazo[1,2-a]pyridines, 5-aryl imidazo[2,1-b]thiazoles, and 3-aryl benzo[d]imidazo[2,1-b][1,3]thiazoles is described by the reaction of phenacyl bromide with heterocyclic amine in the presence of DABCO
Publikováno v:
Tetrahedron Letters. 54:2296-2302
An efficient four-component protocol is described for the synthesis of diversely functionalized pyrroles under catalyst-free condition by using ionic liquid as a reaction media. The developed method is mild, high yielding, and amenable for a variety
Publikováno v:
Tetrahedron Letters. 53:5265-5269
Substituted 2-aminothiazole derivatives were obtained as a result of N -methylimidazole catalyzed cyclization of α-halo ketone carbonyls with ammonium thiocyanate in water–alcoholic media. The generality of the method has been demonstrated by scre
Publikováno v:
Tetrahedron Letters. 53:1780-1785
A very rapid, convenient, and general method for the synthesis of α-oxo thiocyanates has been described by using clay supported ammonium thiocyanate. The procedure avoids the use of additional catalyst, solvent, aqueous work-up and the yields are hi
Publikováno v:
ChemInform. 45
A mild and novel approach is described for the synthesis of functionalized fused imidazole analogues in solvent-free and catalyst-free condition in ionic liquid. The short reaction time, good isolated yields, generality and environmentally benign rea