Electrochemical Synthesis of 3,5-Disubstituted-1,2,4-thiadiazoles through NH4 I-Mediated Dimerization of Thioamides

Electrosynthesis of Trisubstituted 2-Oxazolines via Dehydrogenative Cyclization of β-Amino Arylketones

(2018) Huiqiao Wang et al.   ORGANIC LETTERS

Electrochemical Oxidative Cross-coupling with Hydrogen Evolution: A Green and Sustainable Way for Bond Formation

(2018) Shan Tang et al.   Chem

Building 1,2,4-Thiadiazole: Ten Years of Progress

(2017) Luís M. T. Frija et al.   EUROPEAN JOURNAL OF ORGANIC CHEMISTRY

Catalyst-free synthesis of fused 1,2,3-triazole and isoindoline derivatives via an intramolecular azide–alkene cascade reaction

(2017) Yu-Yang Xie et al.   GREEN CHEMISTRY

Electrochemical intramolecular dehydrogenative C–S bond formation for the synthesis of benzothiazoles

(2017) Pan Wang et al.   GREEN CHEMISTRY

Synthesis of 5-Amino and 3,5-Diamino Substituted 1,2,4-Thiadiazoles by I2-Mediated Oxidative N–S Bond Formation

(2017) Bingnan Wang et al.   JOURNAL OF ORGANIC CHEMISTRY

Electrochemical Cobalt-Catalyzed C–H Oxygenation at Room Temperature

(2017) Nicolas Sauermann et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Metal- and Reagent-Free Intramolecular Oxidative Amination of Tri- and Tetrasubstituted Alkenes

(2017) Peng Xiong et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Electrooxidative Tandem Cyclization of Activated Alkynes with Sulfinic Acids To Access Sulfonated Indenones

(2017) Jiangwei Wen et al.   ORGANIC LETTERS

Multicomponent reactions (MCRs) of arylmethyl bromides, arylamidines and elemental sulfur toward unsymmetric 3,5-diaryl 1,2,4-thiadiazoles

(2017) Zhen Zhou et al.   TETRAHEDRON LETTERS

Palladium(ii)-catalyzed C–C and C–O bond formation for the synthesis of C1-benzoyl isoquinolines from isoquinoline N-oxides and nitroalkenes

(2016) Jiu-ling Li et al.   CHEMICAL COMMUNICATIONS

Electrochemical C–H functionalization and subsequent C–S and C–N bond formation: paired electrosynthesis of 3-amino-2-thiocyanato-α,β-unsaturated carbonyl derivatives mediated by bromide ions

(2016) Li-Shuo Kang et al.   GREEN CHEMISTRY

A Three-Component Approach to 3,5-Diaryl-1,2,4-thiadiazoles under Transition-Metal-Free Conditions

(2016) Hao Xie et al.   ORGANIC LETTERS

High yielding protocol for oxidative dimerization of primary thioamides: a strategy toward 3,5-disubstituted 1,2,4-thiadiazoles

(2016) G. Vanajatha et al.   TETRAHEDRON LETTERS

Electrochemical and In Situ Spectroscopic Evidences toward Empowering Ruthenium-Based Chalcogenides as Solid Acid Fuel Cell Cathodes

(2016) Shraboni Ghoshal et al.   ACS Catalysis

Synthesis of the 1,2,4-thiadiazole alkaloids polycarpathiamines A and B

(2016) Emma K. Davison et al.   Organic Chemistry Frontiers

A facile synthesis of 2,5-disubstituted oxazoles via a copper-catalyzed cascade reaction of alkenes with azides

(2015) Jiu-ling Li et al.   CHEMICAL COMMUNICATIONS

Preparation, structure, and versatile reactivity of pseudocyclic benziodoxole triflate, new hypervalent iodine reagent

(2015) Akira Yoshimura et al.   CHEMICAL COMMUNICATIONS

Oxidative Coupling between Two Hydrocarbons: An Update of Recent C–H Functionalizations

(2015) Chao Liu et al.   CHEMICAL REVIEWS

External Oxidant-Free Oxidative Cross-Coupling: A Photoredox Cobalt-Catalyzed Aromatic C–H Thiolation for Constructing C–S Bonds

(2015) Guoting Zhang et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Redox catalysis in organic electrosynthesis: basic principles and recent developments

(2014) Robert Francke et al.   CHEMICAL SOCIETY REVIEWS

Copper(II)-Mediated Homocoupling of Thioamides for the Synthesis of 1,2,4-Thiadiazoles

(2014) Yadong Sun et al.   EUROPEAN JOURNAL OF ORGANIC CHEMISTRY

Palladium-catalyzed synthesis of benzoxazoles by the cleavage reaction of carbon–carbon triple bonds with o-aminophenol

(2014) Hou-Zhi Xie et al.   GREEN CHEMISTRY

A randomized trial of cefozopran versus cefepime as empirical antibiotic treatment of febrile neutropenia in pediatric cancer patients

(2014) Takeo Sarashina et al.   PEDIATRIC BLOOD & CANCER

New Cytotoxic 1,2,4-Thiadiazole Alkaloids from the Ascidian Polycarpa aurata

(2013) Cong-Dat Pham et al.   ORGANIC LETTERS

Samarium(III)-Catalyzed C(sp3)–H Bond Activation: Synthesis of Indolizines via C–C and C–N Coupling between 2-Alkylazaarenes and Propargylic Alcohols

(2013) Xu Wang et al.   ORGANIC LETTERS

Overcoming the “Oxidant Problem”: Strategies to Use O2 as the Oxidant in Organometallic C–H Oxidation Reactions Catalyzed by Pd (and Cu)

(2012) Alison N. Campbell et al.   ACCOUNTS OF CHEMICAL RESEARCH

Thiadiazole-a Promising Structure in Medicinal Chemistry

(2012) Yijing Li et al.   ChemMedChem

Suzuki-Miyaura Coupling Reactions of 3,5-Dichloro-1,2,4-thiadiazole

(2012) David W. Boykin et al.   HETEROCYCLES

A novel process for the synthesis of 3,5-diaryl-1,2,4-thiadiazoles from aryl nitriles

(2012) Jalil Noei et al.   TETRAHEDRON LETTERS

Optimizing thiadiazole analogues of resveratrol versus three chemopreventive targets

(2011) Abdelrahman S. Mayhoub et al.   BIOORGANIC & MEDICINAL CHEMISTRY

Synthesis and in-vitro anticancer activity of 3,5-bis(indolyl)-1,2,4-thiadiazoles

(2011) Dalip Kumar et al.   BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

Bond Formations between Two Nucleophiles: Transition Metal Catalyzed Oxidative Cross-Coupling Reactions

(2011) Chao Liu et al.   CHEMICAL REVIEWS

Synthesis and anticancer activity of 5-(3-indolyl)-1,3,4-thiadiazoles

(2010) Dalip Kumar et al.   EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

Thiadiazole Carbamates: Potent Inhibitors of Lysosomal Acid Lipase and Potential Niemann−Pick Type C Disease Therapeutics

(2010) Anton I. Rosenbaum et al.   JOURNAL OF MEDICINAL CHEMISTRY

Design, Synthesis, and Structure−Activity Relationship of Substrate Competitive, Selective, and in Vivo Active Triazole and Thiadiazole Inhibitors of the c-Jun N-Terminal Kinase

(2009) Surya K. De et al.   JOURNAL OF MEDICINAL CHEMISTRY

Iodoxolone-Based Hypervalent Iodine Reagents

(2009) Azhar-ul-Haq A. Shah et al.   ORGANIC LETTERS

Modern Strategies in Electroorganic Synthesis

(2008) Jun-ichi Yoshida et al.   CHEMICAL REVIEWS