Literature DB >> 20209543

Asymmetric organocatalysis with sulfones.

Martin Nielsen1, Christian Borch Jacobsen, Nicole Holub, Marcio Weber Paixão, Karl Anker Jørgensen.   

Abstract

Asymmetric organocatalysis has become a powerful tool for the synthesis of optically active compounds. Whereas early research mainly focused on combining simple reagents as a proof-of-concept for asymmetric organocatalysis, recent investigations are directed towards extending the concept to more target- and diversity-oriented synthesis. As a result of the many transformation possibilities and their ability to generate both nucleophilic and electrophilic reaction partners, sulfones have become especially important substrates in the field of organocatalysis.

Entities:  

Year:  2010        PMID: 20209543     DOI: 10.1002/anie.200906340

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


  9 in total

1.  N-heterocyclic carbene-catalyzed rearrangements of vinyl sulfones.

Authors:  Roxanne L Atienza; Howard S Roth; Karl A Scheidt
Journal:  Chem Sci       Date:  2011-06-10       Impact factor: 9.825

Review 2.  The ever-expanding role of asymmetric covalent organocatalysis in scalable, natural product synthesis.

Authors:  Mikail E Abbasov; Daniel Romo
Journal:  Nat Prod Rep       Date:  2014-10       Impact factor: 13.423

Review 3.  Chalcone: A Privileged Structure in Medicinal Chemistry.

Authors:  Chunlin Zhuang; Wen Zhang; Chunquan Sheng; Wannian Zhang; Chengguo Xing; Zhenyuan Miao
Journal:  Chem Rev       Date:  2017-05-10       Impact factor: 60.622

4.  N-Heterocyclic Carbene-Promoted Rauhut]Currier Reactions between Vinyl Sulfones and α,β-Unsaturated Aldehydes.

Authors:  Roxanne L Atienza; Karl A Scheidt
Journal:  Aust J Chem       Date:  2011-08-19       Impact factor: 1.321

5.  Synthesis and biological activities of novel trifluoromethylpyridine amide derivatives containing sulfur moieties.

Authors:  S X Guo; F He; A L Dai; R F Zhang; S H Chen; J Wu
Journal:  RSC Adv       Date:  2020-09-28       Impact factor: 4.036

6.  1-[2,2-Bis(phenyl-sulfon-yl)ethen-yl]-4-meth-oxy-benzene.

Authors:  Haruyasu Asahara; Peter Mayer; Herbert Mayr
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-01-21

7.  2-(4-Meth-oxy-benzyl-idene)-2H-1,3-benzodithiole 1,1,3,3-tetra-oxide.

Authors:  Haruyasu Asahara; Peter Mayer; Herbert Mayr
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-02-04

Review 8.  Molecular targets and anticancer activity of quinoline-chalcone hybrids: literature review.

Authors:  Mamdouh F A Mohamed; Gamal El-Din A Abuo-Rahma
Journal:  RSC Adv       Date:  2020-08-21       Impact factor: 4.036

9.  A Titanium-Catalyzed Reductive α-Desulfonylation.

Authors:  Christoph Kern; Jan Selau; Jan Streuff
Journal:  Chemistry       Date:  2021-03-05       Impact factor: 5.236

  9 in total

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