G. Mahender

发表

A Facile Zn-mediated Stereoselective Synthesis of (E)- and (Z)-Trisubstituted Alkenes from Baylis–Hillman Adducts in Water and Its Application

J. Banerjee, B. Das, A. Majhi, 2006 .

A simple and efficient method for α-bromination of carbonyl compounds using N-bromosuccinimide in the presence of silica-supported sodium hydrogen sulfate as a heterogeneous catalyst

B. Das, Katta Venkateswarlu, I. Mahender, 2005 .

A simple, mild and efficient procedure for selective cleavage of prenyl esters using silica-supported sodium hydrogen sulphate as a heterogenous catalyst☆

B. Das, C. Ramesh, N. Ravindranath, 2003 .

Chemoselective deprotection of trityl ethers using silica-supported sodium hydrogen sulfate ∗

B. Das, Nikhil Chowdhury, G. Mahender, 2004 .

A Convenient, Rapid and Eco-Friendly Synthesis of Bis-indolylmethanes under Microwave Irradiation.

J. Banerjee, B. Das, Katta Venkateswarlu, 2005 .

Synthesis of coumarins via a Pechmann condensation using heterogeneous catalysts1

B. Das, Harish Holla, Katta Venkateswarlu, 2004 .

A Simple and Facile Chemo- and Regioselective Deprotection of Acetonides Using Silica Supported Sodium Hydrogen Sulfate as a Heterogeneous Catalyst

B. Das, C. Ramesh, R. Ramu, 2003 .

Simple, Mild and Efficient Thioacetalization and Transthioacetalization of Carbonyl Compounds and Deprotection of Thioacetals: Unique Role of Thiols in the Selectivity of Thioacetalization

B. Das, R. Ramu, M. R. Reddy, 2005 .

Organic reactions in water: an efficient zinc-mediated stereoselective synthesis of (E)- and (Z)-trisubstituted alkenes using unactivated alkyl halides.

J. Banerjee, B. Das, A. Majhi, 2004, Organic letters.

Synthetic Applications of the Baylis-Hillman Reaction: Simple and Convenient Synthesis of Five Important Insect Pheromones

J. Banerjee, B. Das, A. Majhi, 2006 .

An efficient stereoselective synthesis of (E)- and (Z)-trisubstituted alkenes from unactivated Baylis–Hillman adducts using NaBH4/CuCl2·2H2O

J. Banerjee, B. Das, A. Majhi, 2004 .

Hypervalent iodine-mediated interaction of aldoximes with activated alkenes including Baylis–Hillman adducts: a new and efficient method for the preparation of nitrile oxides from aldoximes☆

J. Banerjee, B. Das, Harish Holla, 2004 .

A mild, highly selective and remarkably easy procedure for deprotection of aromatic acetates using ammonium acetate as a neutral catalyst in aqueous medium☆

B. Das, C. Ramesh, N. Ravindranath, 2003 .

An easy access to chromano-isoxazolines and functionalized isoxazolines

J. Banerjee, B. Das, Harish Holla, 2004 .

Studies on Novel Synthetic Methodologies. Part 72. A Facile Zn‐Mediated Stereoselective Synthesis of (E)‐ and (Z)‐Trisubstituted Alkenes from Baylis—Hillman Adducts in Water and Its Application.

J. Banerjee, B. Das, A. Majhi, 2006 .

Cleomiscosin A, a coumarino-lignoid from Jatropha gossypifolia.

B. Das, B. Venkataiah, A. Kashinatham, 2003 .

Deoxypreussomerins from Jatropha curcas: are they also plant metabolites?

B. Das, K. R. Kumar, N. Ravindranath, 2004, Phytochemistry.

A Convenient Method for the Preparation of Benzopyrano- and Furopyrano-2-isoxazoline Derivatives Using Hypervalent Iodine Reagents

B. Bandgar, B. Das, Harish Holla, 2005 .

A convenient, rapid, highly selective and eco-friendly method for deprotection of aryl acetates using silica gel supported ammonium formate under microwave irradiation

B. Das, C. Ramesh, G. Mahender, 2003 .

Chemical Transformations of Parthenin, a Natural Bioactive Sesquiterpenoid [1]

B. Das, V. S. Reddy, Nisith Bhunia, 2009, Natural product communications.

Amberlyst-15 catalyzed acetylation of heteroaromatics with acetic anhydride under solvent free conditions

J. Banerjee, B. Das, Harish Holla, 2005 .

Pseudoguaianolides from the Flowers of Parthenium hysterophorus

Y. Tzeng, B. Das, K. Ravikumar, 2006 .

(3R*,6S*,6aR*,9S*,9aS*)‐6,6a,9‐Trihydroxy‐3,6,9a‐trimethylperhydroazuleno[1,2‐b]furan‐2‐one

B. Das, K. Ravikumar, G. Swamy, 2005 .

Biflavonoids from Cycas beddomei.

B. Das, B. Jagadeesh, A. Prabhakar, 2005, Chemical and pharmaceutical bulletin.