Literature DB >> 16287179

Organosulfur compounds: electrophilic reagents in transition-metal-catalyzed carbon-carbon bond-forming reactions.

Srinivas Reddy Dubbaka1, Pierre Vogel.   

Abstract

Transition-metal-catalyzed carbon-carbon bond-forming reactions are among the most powerful methods in organic synthesis and play a crucial role in modern materials science and medicinal chemistry. Recent developments in the area of ligands and additives permit the cross-coupling of a large variety of reactants, including inexpensive and readily available sulfonyl chlorides. Their desulfitative carbon-carbon cross-coupling reactions (Negishi, Stille, carbonylative Stille, Suzuki-Miyaura, and Sonogashira-Hagihara-type cross-couplings and Mizoroki-Heck-type arylations) are reviewed together with carbon-carbon cross-coupling reactions with other organosulfur compounds as electrophilic reagents.

Entities:  

Year:  2005        PMID: 16287179     DOI: 10.1002/anie.200463007

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  21 in total

1.  Aryliodine (III) Diacetates as Substrates for Pd-Ag Catalyzed Arylation of Alkenes.

Authors:  Nikolai M Evdokimov; Alexander Kornienko; Igor V Magedov
Journal:  Tetrahedron Lett       Date:  2011-08-17       Impact factor: 2.415

Review 2.  Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners.

Authors:  Ranjan Jana; Tejas P Pathak; Matthew S Sigman
Journal:  Chem Rev       Date:  2011-02-14       Impact factor: 60.622

3.  Nickel-catalyzed reductive conjugate addition to enones via allylnickel intermediates.

Authors:  Ruja Shrestha; Stephanie C M Dorn; Daniel J Weix
Journal:  J Am Chem Soc       Date:  2013-01-08       Impact factor: 15.419

4.  Mobilizing Cu(I) for carbon-carbon bond forming catalysis in the presence of thiolate. Chemical mimicking of metallothioneins.

Authors:  Zhihui Zhang; Matthew G Lindale; Lanny S Liebeskind
Journal:  J Am Chem Soc       Date:  2011-03-30       Impact factor: 15.419

5.  Iron-catalyzed cross-coupling of unactivated secondary alkyl thio ethers and sulfones with aryl Grignard reagents.

Authors:  Scott E Denmark; Alexander J Cresswell
Journal:  J Org Chem       Date:  2013-11-20       Impact factor: 4.354

6.  Efficient synthesis of 3-sulfolenes from allylic alcohols and 1,3-dienes enabled by sodium metabisulfite as a sulfur dioxide equivalent.

Authors:  Hang T Dang; Vu T Nguyen; Viet D Nguyen; Hadi D Arman; Oleg V Larionov
Journal:  Org Biomol Chem       Date:  2018-05-15       Impact factor: 3.876

7.  Enantioselective Synthesis of Biaryl Atropisomers via the Addition of Thiophenols into Aryl-Naphthoquinones.

Authors:  Sean M Maddox; Gregory A Dawson; Nicholas C Rochester; Arianna B Ayonon; Curtis E Moore; Arnold L Rheingold; Jeffrey L Gustafson
Journal:  ACS Catal       Date:  2018-05-08       Impact factor: 13.084

8.  Mechanistic Insights into the Aerobic Cu(I)-Catalyzed Cross-Coupling of S-Acyl Thiosalicylamide Thiol Esters and Boronic Acids.

Authors:  Adrián Varela-Álvarez; Lanny S Liebeskind; Djamaladdin G Musaev
Journal:  Organometallics       Date:  2012-08-15       Impact factor: 3.876

9.  Highly Stereoselective and Catalytic Desulfitative C-O and C-I Dienylation with Sulfolenes: the Importance of Basic Additives.

Authors:  Hang T Dang; Viet D Nguyen; Hoang H Pham; Hadi D Arman; Oleg V Larionov
Journal:  Tetrahedron       Date:  2019-04-08       Impact factor: 2.457

10.  Highly Regio- and Stereoselective Catalytic Synthesis of Conjugated Dienes and Polyenes.

Authors:  Vu T Nguyen; Hang T Dang; Hoang H Pham; Viet D Nguyen; Carsten Flores-Hansen; Hadi D Arman; Oleg V Larionov
Journal:  J Am Chem Soc       Date:  2018-06-26       Impact factor: 15.419

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