Photoredox-catalyzed synthesis of sulfonated oxazolines from N-allylamides through the insertion of sulfur dioxide

Copper-Catalyzed Regioselective 1,4-Selenosulfonylation of 1,3-Enynes to Access Cyanoalkylsulfonylated Allenes

(2021) Fu-Sheng He et al.   ORGANIC LETTERS

Metal-Free Sulfonylative Spirocyclization of Indolyl-ynones via Insertion of Sulfur Dioxide: Access to Sulfonated Spiro[cyclopentenone-1,3′-indoles]

(2021) Zhichao Chen et al.   ORGANIC LETTERS

Improved Synthetic Method for 5-[(Phenylthio)methyl]oxazoline Derivatives: Electrophilic Cyclization of Allylic Amide Using a Brønsted Acid and Tetrabutylammonium Chloride under Mild Conditions

(2020) Yoshihiro Nagao et al.   SYNLETT

Regio- and Enantioselective Bromocyclization of Difluoroalkenes as a Strategy to Access Tetrasubstituted Difluoromethylene-Containing Stereocenters

(2020) Edward Miller et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Visible-Light-Mediated Ru-Catalyzed Synthesis of 3-(Arylsulfonyl)but-3-enals via Coupling of α-Allenols with Diazonium Salts and Sulfur Dioxide

(2020) Fernando Herrera et al.   ORGANIC LETTERS

Preparation of Heterocycles via Visible-Light-Driven Aerobic Selenation of Olefins with Diselenides

(2019) Qing-Bao Zhang et al.   ORGANIC LETTERS

Visible-light-promoted sulfonylmethylation of imidazopyridines

(2019) Xia Mi et al.   CHINESE CHEMICAL LETTERS

The concept of dual roles design in clean organic preparation

(2019) Zhong Cao et al.   CHINESE CHEMICAL LETTERS

Multicomponent Reductive Cross-Coupling of an Inorganic Sulfur Dioxide Surrogate: Straightforward Construction of Diversely Functionalized Sulfones

(2019) Yingying Meng et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Completely Stereoselective Synthesis of Sulfonated 1,3-Dihydroisobenzofurans via Radical Multicomponent Reactions

(2019) Hao-Nan Shi et al.   JOURNAL OF ORGANIC CHEMISTRY

Generation of sulfonated 1-isoindolinones through a multicomponent reaction with the insertion of sulfur dioxide

(2018) Jun Zhang et al.   CHEMICAL COMMUNICATIONS

Generation of sulfonated isobenzofuran-1(3H)-ones under photocatalysis through the insertion of sulfur dioxide

(2018) Jun Zhang et al.   Organic Chemistry Frontiers

Analysis of US FDA-Approved Drugs Containing Sulfur Atoms

(2018) Kevin A. Scott et al.   Topics in Current Chemistry

A comprehensive overview of directing groups applied in metal-catalysed C–H functionalisation chemistry

(2018) Carlo Sambiagio et al.   CHEMICAL SOCIETY REVIEWS

Electrochemical Fluorocyclization of N-Allylcarboxamides to 2-Oxazolines by Hypervalent Iodine Mediator

(2018) John D. Haupt et al.   ORGANIC LETTERS

Copper(II)-Catalyzed Reaction of 2,3-Allenoic Acids, Sulfur Dioxide, and Aryldiazonium Tetrafluoroborates: Route to 4-Sulfonylated Furan-2(5H)-ones

(2018) Kaida Zhou et al.   ORGANIC LETTERS

Synthesis of CF 3 -containing oxazolines via trifluoromethylation of allylamides with Togni reagent in the presence of alkali metal iodides

(2017) Shintaro Kawamura et al.   JOURNAL OF FLUORINE CHEMISTRY

Iridium(III)-Catalyzed One-Pot Access to 1,2-Disubstituted Benzimidazoles Starting from Imidamides and Sulfonyl Azides

(2017) Linhua Xu et al.   ORGANIC LETTERS

Ag-Catalyzed Oxidative Cyclization Reaction of 1,6-Enynes and Sodium Sulfinate: Access to Sulfonylated Benzofurans

(2017) Wanqing Wu et al.   ORGANIC LETTERS

Palladium-Catalyzed Direct C–H Functionalization of Indoles with the Insertion of Sulfur Dioxide: Synthesis of 2-Sulfonated Indoles

(2017) Tong Liu et al.   ORGANIC LETTERS

Generation of Sulfonyl Radicals from Aryldiazonium Tetrafluoroborates and Sulfur Dioxide: The Synthesis of 3-Sulfonated Coumarins

(2016) Danqing Zheng et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Iodine-promoted cyclization of N-propynyl amides and N-allyl amides via sulfonylation and sulfenylation

(2016) Gopal Chandru Senadi et al.   CHEMICAL COMMUNICATIONS

Sulfur Containing Scaffolds in Drugs: Synthesis and Application in Medicinal Chemistry

(2016) Minghao Feng et al.   CURRENT TOPICS IN MEDICINAL CHEMISTRY

Cu-Catalyzed Deoxygenative C2-Sulfonylation Reaction of Quinoline N-Oxides with Sodium Sulfinate

(2016) Bingnan Du et al.   ORGANIC LETTERS

Generation of N-aminosulfonamides via a photo-induced fixation of sulfur dioxide into aryl/alkyl halides

(2016) Yuewen Li et al.   Organic Chemistry Frontiers

Copper-triggered three-component reaction of CF3CHN2, nitriles, and aldehydes: highly diastereoselective synthesis of CF3-substituted oxazolines and vicinal amino alcohols

(2015) Ai-Jie Cai et al.   CHEMICAL COMMUNICATIONS

Modular Preparation of 5-Halomethyl-2-oxazolines via PhI(OAc)2-Promoted Intramolecular Halooxygenation of N-Allylcarboxamides

(2015) Gong-Qing Liu et al.   JOURNAL OF ORGANIC CHEMISTRY

Fixation of sulfur dioxide into small molecules

(2015) Gang Liu et al.   ORGANIC & BIOMOLECULAR CHEMISTRY

Iodoarene-Catalyzed Cyclizations of Unsaturated Amides

(2015) Ali Alhalib et al.   ORGANIC LETTERS

Pd(II)-Catalyzed Direct Sulfonylation of Unactivated C(sp3)–H Bonds with Sodium Sulfinates

(2015) Wei-Hao Rao et al.   ORGANIC LETTERS

The Development and Application of Sulfur Dioxide Surrogates in Synthetic Organic Chemistry

(2015) Edward J. Emmett et al.   Asian Journal of Organic Chemistry

Transition Metal-Free Trifluoromethylation ofN-Allylamides with Sodium Trifluoromethanesulfinate: Synthesis of Trifluoromethyl-Containing Oxazolines

(2014) Jipan Yu et al.   ADVANCED SYNTHESIS & CATALYSIS

Application of Fundamental Organometallic Chemistry to the Development of a Gold-Catalyzed Synthesis of Sulfinate Derivatives

(2014) Miles W. Johnson et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Synthesis of 2-Oxazolines by in Situ Desilylation and Cyclodehydration of β-Hydroxyamides

(2014) Marco Brandstätter et al.   JOURNAL OF ORGANIC CHEMISTRY

Synthesis of 2-Aryl/Heteroaryloxazolines from Nitriles under Metal- and Catalyst-Free Conditions and Evaluation of Their Antioxidant Activities

(2014) Parul Garg et al.   JOURNAL OF ORGANIC CHEMISTRY

One-Pot Access to Sulfonylmethyl Arylpyrroles via the Domino Aerobic Wacker-Type Aminocyclization/1,4-Sulfonyl Migration

(2014) Meng-Yang Chang et al.   ORGANIC LETTERS

Base-Catalyzed Cyclization of N-Sulfonyl Propargylamides to Sulfonylmethyl-Substituted Oxazoles via Sulfonyl Migration

(2013) Xinzhang Yu et al.   JOURNAL OF ORGANIC CHEMISTRY

Enantioselective Chlorocyclization of Indole Derived Benzamides for the Synthesis of Spiro-indolines

(2013) Qin Yin et al.   ORGANIC LETTERS

Sulfonylation of Quinoline N-Oxides with Aryl Sulfonyl Chlorides via Copper-Catalyzed C–H Bonds Activation

(2013) Zhiyong Wu et al.   ORGANIC LETTERS

A Catalytic Asymmetric Chlorocyclization of Unsaturated Amides

(2011) Arvind Jaganathan et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Structure–activity relationship of new anti-tuberculosis agents derived from oxazoline and oxazole benzyl esters

(2010) Garrett C. Moraski et al.   EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

Synthesis of 2-oxazolines via boron esters of N-(2-hydroxyethyl) amides

(2010) Baris Ilkgul et al.   TETRAHEDRON LETTERS

Recent Applications of Oxazoline-Containing Ligands in Asymmetric Catalysis

(2009) Gráinne C. Hargaden et al.   CHEMICAL REVIEWS

Evolving Organic Synthesis Fostered by the Pluripotent Phenylsulfone Moiety

(2009) Ahmad El-Awa et al.   CHEMICAL REVIEWS

Synthesis, characterization and evaluation of antibacterial activity of some thiazolo[3,2-b][1,2,4]triazole incorporating diphenylsulfone moieties☆

(2009) Stefania-Felicia Barbuceanu et al.   EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

Activation ofN-Sulfonyl Oxaziridines Using Copper(II) Catalysts: Aminohydroxylations of Styrenes and 1,3-Dienes

(2008) David J. Michaelis et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Shahidine, a novel and highly labile oxazoline from Aegle marmelos: the parent compound of aegeline and related amides

(2008) Shaheen Faizi et al.   TETRAHEDRON

Silica sulfuric acid: A versatile and reusable heterogeneous catalyst for the synthesis of oxazolines and imidazolines under various reaction conditions

(2007) Iraj Mohammadpoor-Baltork et al.   CATALYSIS COMMUNICATIONS