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Results: 1-25 | 26-48
Results: 1-25/48
Selective and rapid oxidation of primary, allylic and benzylic alcohols tothe corresponding carbonyl compounds with NaNO2-acetic anhydride under mild and solvent-free conditions (vol 1, pg 3559, 2000)
Authors: Bandgar, BP Sadavarte, VS Uppalla, LS
Citation: Bp. Bandgar et al., Selective and rapid oxidation of primary, allylic and benzylic alcohols tothe corresponding carbonyl compounds with NaNO2-acetic anhydride under mild and solvent-free conditions (vol 1, pg 3559, 2000), J CHEM S P1, (9), 2001, pp. 1151-1151
Montmorillonite K-10 catalyzed synthesis of beta-keto esters: condensationof ethyl diazoacetate with aldehydes under mild conditions
Authors: Bandgar, BP Pandit, SS Sadavarte, VS
Citation: Bp. Bandgar et al., Montmorillonite K-10 catalyzed synthesis of beta-keto esters: condensationof ethyl diazoacetate with aldehydes under mild conditions, GREEN CHEM, 3(5), 2001, pp. 247-249
Organic reactions in aqueous medium: FeF3 catalyzed chemoselective addition of cyanotrimethylsilane to aldehydes
Authors: Bandgar, BP Kamble, VT
Citation: Bp. Bandgar et Vt. Kamble, Organic reactions in aqueous medium: FeF3 catalyzed chemoselective addition of cyanotrimethylsilane to aldehydes, GREEN CHEM, 3(5), 2001, pp. 265-266
Envirocat EPZG and natural clay as efficient catalysts for transesterification of beta-keto esters
Authors: Bandgar, BP Uppalla, LS Sadavarte, VS
Citation: Bp. Bandgar et al., Envirocat EPZG and natural clay as efficient catalysts for transesterification of beta-keto esters, GREEN CHEM, 3(1), 2001, pp. 39-41
Lithium perchlorate as an efficient catalyst for selective transesterification of beta-keto esters essentially under neutral conditions
Authors: Bandgar, BP Sadavarte, VS Uppalla, LS
Citation: Bp. Bandgar et al., Lithium perchlorate as an efficient catalyst for selective transesterification of beta-keto esters essentially under neutral conditions, SYNLETT, (8), 2001, pp. 1338-1340
Chemoselective transesterification of beta-keto esters under neutral conditions using NBS as a catalyst
Authors: Bandgar, BP Uppalla, LS Sadavarte, VS
Citation: Bp. Bandgar et al., Chemoselective transesterification of beta-keto esters under neutral conditions using NBS as a catalyst, SYNLETT, (11), 2001, pp. 1715-1718
Sodium perborate catalyzed selective transesterification of beta-keto esters under neutral conditions
Authors: Bandgar, BP Sadavarte, VS Uppalla, LS
Citation: Bp. Bandgar et al., Sodium perborate catalyzed selective transesterification of beta-keto esters under neutral conditions, CHEM LETT, (9), 2001, pp. 894-895
Sulfurated borohydride exchange resin: reductive cleavage of aryl acetatesunder mild conditions
Authors: Bandgar, BP Kamble, VT
Citation: Bp. Bandgar et Vt. Kamble, Sulfurated borohydride exchange resin: reductive cleavage of aryl acetatesunder mild conditions, J CHEM R-S, (2), 2001, pp. 54-55
Zn mediated transesterification of beta-ketoesters
Authors: Bandgar, BP Sadavarte, VS Uppalla, LS
Citation: Bp. Bandgar et al., Zn mediated transesterification of beta-ketoesters, J CHEM R-S, (1), 2001, pp. 16-17
A mild procedure for rapid and selective deprotection of aryl acetates using natural kaolinitic clay as a reusable catalyst
Authors: Bandgar, BP Uppalla, LS Sagar, AD Sadavarte, VS
Citation: Bp. Bandgar et al., A mild procedure for rapid and selective deprotection of aryl acetates using natural kaolinitic clay as a reusable catalyst, TETRAHEDR L, 42(6), 2001, pp. 1163-1165
An expedient and highly selective iodination of alcohols using a KI/BF3 center dot Et2O system
Authors: Bandgar, BP Sadavarte, VS Uppalla, LS
Citation: Bp. Bandgar et al., An expedient and highly selective iodination of alcohols using a KI/BF3 center dot Et2O system, TETRAHEDR L, 42(5), 2001, pp. 951-953
Reduction of sulfur with borohydride exchange resin in methanol: application to rapid and selective synthesis of disulfides
Authors: Bandgar, BP Uppalla, LS Sadavarte, VS
Citation: Bp. Bandgar et al., Reduction of sulfur with borohydride exchange resin in methanol: application to rapid and selective synthesis of disulfides, TETRAHEDR L, 42(38), 2001, pp. 6741-6743
Zinc-mediated fast sulfonylation of aromatics
Authors: Bandgar, BP Kasture, SP
Citation: Bp. Bandgar et Sp. Kasture, Zinc-mediated fast sulfonylation of aromatics, SYN COMMUN, 31(7), 2001, pp. 1065-1068
Sulfurated borohydride exchange resin: A novel reagent for selective reduction of aldehydes
Authors: Bandgar, BP Kamble, VT
Citation: Bp. Bandgar et Vt. Kamble, Sulfurated borohydride exchange resin: A novel reagent for selective reduction of aldehydes, SYN COMMUN, 31(19), 2001, pp. 3037-3040
Chemoselective acetylation of alcohols, amines, and thiols without catalyst and solvent
Authors: Bandgar, BP Kasture, SP Kamble, VT
Citation: Bp. Bandgar et al., Chemoselective acetylation of alcohols, amines, and thiols without catalyst and solvent, SYN COMMUN, 31(15), 2001, pp. 2255-2259
Metal salts as novel catalysts for efficient transesterification of beta-ketoesters
Authors: Bandgar, BP Sadavarte, VS Uppalla, LS
Citation: Bp. Bandgar et al., Metal salts as novel catalysts for efficient transesterification of beta-ketoesters, SYN COMMUN, 31(13), 2001, pp. 2063-2066
Chemoselective protection of hydroxyl groups and deprotection of silyl ethers
Authors: Bandgar, BP Kasture, SP
Citation: Bp. Bandgar et Sp. Kasture, Chemoselective protection of hydroxyl groups and deprotection of silyl ethers, MONATS CHEM, 132(9), 2001, pp. 1101-1104
Chemoselective preparation of oximes, semicarbazones, and tosylhydrazones without catalyst and solvent
Authors: Bandgar, BP Sadavarte, VS Uppalla, LS Govande, R
Citation: Bp. Bandgar et al., Chemoselective preparation of oximes, semicarbazones, and tosylhydrazones without catalyst and solvent, MONATS CHEM, 132(3), 2001, pp. 403-406
Simple protocol for synthesis and cleavage of tetrahydropyranyl ethers using FeSO4 as an inexpensive catalyst
Authors: Bandgar, BP Kasture, SP
Citation: Bp. Bandgar et Sp. Kasture, Simple protocol for synthesis and cleavage of tetrahydropyranyl ethers using FeSO4 as an inexpensive catalyst, J CHIN CHEM, 48(5), 2001, pp. 877-878
Selective and rapid oxidation of primary, allylic and benzylic alcohols tothe corresponding carbonyl compounds with NaNO2-acetic anhydride under mild and solvent-free conditions
Authors: Bandgar, BP Sadavarte, VS Uppalla, LS
Citation: Bp. Bandgar et al., Selective and rapid oxidation of primary, allylic and benzylic alcohols tothe corresponding carbonyl compounds with NaNO2-acetic anhydride under mild and solvent-free conditions, J CHEM S P1, (21), 2000, pp. 3559-3560
Envirocat EPZG((R)) catalysis: an efficient and rapid procedure for the deprotection of 1,1-diacetates without solvent
Authors: Bandgar, BP Kasture, SP Tidke, K Makone, SS
Citation: Bp. Bandgar et al., Envirocat EPZG((R)) catalysis: an efficient and rapid procedure for the deprotection of 1,1-diacetates without solvent, GREEN CHEM, 2(4), 2000, pp. 152-153
Natural kaolinitic clay: a remarkable reusable solid catalyst for the selective cleavage of thioacetals without solvent
Authors: Bandgar, BP Kasture, SP
Citation: Bp. Bandgar et Sp. Kasture, Natural kaolinitic clay: a remarkable reusable solid catalyst for the selective cleavage of thioacetals without solvent, GREEN CHEM, 2(4), 2000, pp. 154-156
Ferrous sulfate catalyzed synthesis of 2-oxazolines from nitriles
Authors: Bandgar, BP Kasture, SP Aherwadkar, AP
Citation: Bp. Bandgar et al., Ferrous sulfate catalyzed synthesis of 2-oxazolines from nitriles, I J HET CHE, 10(2), 2000, pp. 105-108
Clean and efficient synthesis of thioethers under mild and non-aqueous conditions
Authors: Bandgar, BP Sadavarte, VS Pawar, SG Kamble, VT
Citation: Bp. Bandgar et al., Clean and efficient synthesis of thioethers under mild and non-aqueous conditions, I J HET CHE, 10(2), 2000, pp. 159-160
One pot rapid synthesis of thiols from alcohols under mild conditions
Authors: Bandgar, BP Sadavarte, VS
Citation: Bp. Bandgar et Vs. Sadavarte, One pot rapid synthesis of thiols from alcohols under mild conditions, SYNLETT, (6), 2000, pp. 908-910
Risultati: 1-25 | 26-48