Microwave-assisted synthesis of 3-sulfenylindoles by sulfonyl hydrazides using organic ionic base-Brønsted acid

Synthesis of 2-Aryl and 3-Aryl Benzo[b]furan Thioethers Using Aryl Sulfonyl Hydrazides as Sulfenylation Reagents

(2015) Xia Zhao et al.   JOURNAL OF ORGANIC CHEMISTRY

Iodine-catalyzed regioselective thiolation of imidazo[1,2-a]pyridines using sulfonyl hydrazides as a thiol surrogate

(2015) Avik Kumar Bagdi et al.   ORGANIC & BIOMOLECULAR CHEMISTRY

A Direct Metal-Free Decarboxylative Sulfono Functionalization (DSF) of Cinnamic Acids to α,β-Unsaturated Phenyl Sulfones

(2015) Rahul Singh et al.   ORGANIC LETTERS

Metal free sulfenylation of active methylene compounds and indole: TBATB mediated synthesis

(2015) Rajjakfur Rahaman et al.   TETRAHEDRON LETTERS

On the existence of and mechanism for microwave-specific reaction rate enhancement

(2015) Gregory B. Dudley et al.   Chemical Science

Rapid Two-Step Synthesis of Benzimidazo[1′,2′:1,5]pyrrolo[2,3-c]isoquinolines by a Three-Component Coupling Reaction

(2014) Bharat D. Narhe et al.   ACS Combinatorial Science

Synthesis of 3-sulfenylated indoles by a simple NaOH promoted sulfenylation reaction

(2014) Yunyun Liu et al.   RSC Advances

Iodine-Catalyzed Regioselective Sulfenylation of Indoles with Sulfonyl Hydrazides

(2013) Fu-Lai Yang et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

K2CO3 promoted direct sulfenylation of indoles: a facile approach towards 3-sulfenylindoles

(2013) Peng Sang et al.   GREEN CHEMISTRY

Convenient MW-Assisted Synthesis of Unsymmetrical Sulfides Using Sulfonyl Hydrazides as Aryl Thiol Surrogate

(2013) Neetu Singh et al.   ORGANIC LETTERS

Regioselective Hydrothiolation of Alkynes by Sulfonyl Hydrazides Using Organic Ionic Base–Brønsted Acid

(2013) Rahul Singh et al.   ORGANIC LETTERS

Microwave Effects in Organic Synthesis: Myth or Reality?

(2012) C. Oliver Kappe et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Tetrabutylammonium iodide catalyzed allylic sulfonylation of α-methyl styrene derivatives with sulfonylhydrazides

(2012) Xiaoqing Li et al.   CHEMICAL COMMUNICATIONS

Transition metal-free direct C–H bond thiolation of 1,3,4-oxadiazoles and related heteroarenes

(2012) Liang-Hua Zou et al.   CHEMICAL COMMUNICATIONS

Palladium-Catalyzed Direct Arylation of N-Heteroarenes with Arylsulfonyl Hydrazides

(2012) Bo Liu et al.   CHEMISTRY-A EUROPEAN JOURNAL

Oxidative Mizoroki-Heck-Type Reaction of Arylsulfonyl Hydrazides for a Highly Regio- and Stereoselective Synthesis of Polysubstituted Alkenes

(2012) Fu-Lai Yang et al.   CHEMISTRY-A EUROPEAN JOURNAL

Hydrogen Bonds: A Structural Insight into Ionic Liquids

(2012) Kun Dong et al.   CHEMISTRY-A EUROPEAN JOURNAL

An Efficient Catalytic Method for Regioselective Sulfenylation of Electron-Rich Aza-Aromatics at Room Temperature

(2012) Enrico Marcantoni et al.   EUROPEAN JOURNAL OF ORGANIC CHEMISTRY

Iodine-catalyzed oxidative system for 3-sulfenylation of indoles with disulfides using DMSO as oxidant under ambient conditions in dimethyl carbonate

(2012) Wenlei Ge et al.   GREEN CHEMISTRY

Palladium-catalyzed desulfitative arylation of azoles with arylsulfonyl hydrazides

(2012) Xinzhang Yu et al.   ORGANIC & BIOMOLECULAR CHEMISTRY

Venting-while-Heating Microwave-Assisted Synthesis of 3-Arylthioindoles

(2012) Giuseppe La Regina et al.   ACS Combinatorial Science

Activation and Deactivation of a Chemical Transformation by an Electromagnetic Field: Evidence for Specific Microwave Effects in the Formation of Grignard Reagents

(2011) Bernhard Gutmann et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Synthesis of di(hetero)aryl sulfides by directly using arylsulfonyl chlorides as a sulfur source

(2011) Qian Wu et al.   CHEMICAL COMMUNICATIONS

Room-Temperature Ionic Liquids: Solvents for Synthesis and Catalysis. 2

(2011) Jason P. Hallett et al.   CHEMICAL REVIEWS

Increasing the Reactivity of Nitrogen Catalysts

(2011) Nicolas De Rycke et al.   CHEMISTRY-A EUROPEAN JOURNAL

A critical assessment of the greenness and energy efficiency of microwave-assisted organic synthesis

(2011) Jonathan D. Moseley et al.   GREEN CHEMISTRY

Iron-catalyzed sulfonyl radical formations from sulfonylhydrazides and oxidative addition to alkenes

(2011) Tsuyoshi Taniguchi et al.   ORGANIC & BIOMOLECULAR CHEMISTRY

An efficient and clean CuI-catalyzed chalcogenylation of aromatic azaheterocycles with dichalcogenides

(2011) Zhen Li et al.   TETRAHEDRON

Toward Understanding the Origin of Positive Effects of Ionic Liquids on Catalysis: Formation of More Reactive Catalysts and Stabilization of Reactive Intermediates and Transition States in Ionic Liquids

(2010) Ji Woong Lee et al.   ACCOUNTS OF CHEMICAL RESEARCH

Parallel Synthesis of Ureas and Carbamates from Amines and CO2under Mild Conditions

(2010) Scott L. Peterson et al.   ORGANIC LETTERS

The use of anhydrous CeCl3 as a catalyst for the synthesis of 3-sulfenyl indoles

(2010) Claudio C. Silveira et al.   TETRAHEDRON LETTERS

New Frontiers in Materials Science Opened by Ionic Liquids

(2009) Tsukasa Torimoto et al.   ADVANCED MATERIALS

DBU Catalysis ofN,N′-Carbonyldiimidazole-Mediated Amidations§

(2009) Claude Larrivée-Aboussafy et al.   ORGANIC LETTERS

Iron(III) Chloride: A Versatile Catalyst for the Practical Synthesis of 3-Sulfenylindoles

(2009) Jhillu Yadav et al.   SYNTHESIS-STUTTGART

Aza-Michael addition of aliphatic or aromatic amines to α,β-unsaturated compounds catalyzed by a DBU-derived ionic liquid under solvent-free conditions

(2009) An-Guo Ying et al.   TETRAHEDRON LETTERS

Microwave-Assisted Organic Synthesis and Transformations using Benign Reaction Media

(2008) Vivek Polshettiwar et al.   ACCOUNTS OF CHEMICAL RESEARCH

3,4-Disubstituted indole acylsulfonamides: A novel series of potent and selective human EP3 receptor antagonists

(2008) Nian Zhou et al.   BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

4-Hydroxy-2-quinolones 145. p-Toluenesulfonylhydrazide as a tosylating agent

(2008) I. V. Ukrainets et al.   Chemistry of Heterocyclic Compounds

Oxone‐Mediated Oxidative 3‐Arylthio Substitution of Indoles

(2008) Guaili Wu et al.   SYNTHETIC COMMUNICATIONS