Literature DB >> 26369815

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

Minghao Feng, Bingqing Tang, Steven H Liang, Xuefeng Jiang1.   

Abstract

The impact of the development of sulfur therapeutics is instrumental to the evolution of the pharmaceutical industry. Sulfur-derived functional groups can be found in a broad range of pharmaceuticals and natural products. For centuries, sulfur continues to maintain its status as the dominating heteroatom integrated into a set of 362 sulfur-containing FDA approved drugs (besides oxygen or nitrogen) through the present. Sulfonamides, thioethers, sulfones and Penicillin are the most common scaffolds in sulfur containing drugs, which are well studied both on synthesis and application during the past decades. In this review, these four moieties in pharmaceuticals and recent advances in the synthesis of the corresponding core scaffolds are presented.

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Year:  2016        PMID: 26369815      PMCID: PMC4877035          DOI: 10.2174/1568026615666150915111741

Source DB:  PubMed          Journal:  Curr Top Med Chem        ISSN: 1568-0266            Impact factor:   3.295


  32 in total

1.  Relative antibacterial activity of three penicillins.

Authors:  L P GARROD
Journal:  Br Med J       Date:  1960-02-20

2.  A well-defined (POCOP)Rh catalyst for the coupling of aryl halides with thiols.

Authors:  Samuel D Timpa; Christopher J Pell; Oleg V Ozerov
Journal:  J Am Chem Soc       Date:  2014-10-10       Impact factor: 15.419

3.  Synthesis of 1-(2,3-dihydrobenzofuran-3-yl)-methanesulfonohydrazides through insertion of sulfur dioxide.

Authors:  Yuanyuan An; Danqing Zheng; Jie Wu
Journal:  Chem Commun (Camb)       Date:  2014-10-11       Impact factor: 6.222

4.  A palladium-catalyzed three-component coupling of arylboronic acids, sulfur dioxide and hydrazines.

Authors:  Shengqing Ye; Jie Wu
Journal:  Chem Commun (Camb)       Date:  2012-06-29       Impact factor: 6.222

5.  Direct cross-coupling access to diverse aromatic sulfide: palladium-catalyzed double C-S bond construction using Na2S2O3 as a sulfurating reagent.

Authors:  Zongjun Qiao; Jianpeng Wei; Xuefeng Jiang
Journal:  Org Lett       Date:  2014-02-06       Impact factor: 6.005

6.  Sulfur dioxide mediated one-pot, three- and four-component syntheses of polyfunctional sulfonamides and sulfonic esters: study of the stereoselectivity of the ene reaction of sulfur dioxide.

Authors:  Laure C Bouchez; Srinivas Reddy Dubbaka; Māris Turks; Pierre Vogel
Journal:  J Org Chem       Date:  2004-09-17       Impact factor: 4.354

7.  Effects of ranitidine and sucralfate on ketoconazole bioavailability.

Authors:  S C Piscitelli; T F Goss; J H Wilton; D T D'Andrea; H Goldstein; J J Schentag
Journal:  Antimicrob Agents Chemother       Date:  1991-09       Impact factor: 5.191

8.  A copper-catalyzed three-component reaction of triethoxysilanes, sulfur dioxide, and hydrazines.

Authors:  Xianbo Wang; Lijun Xue; Zhiyong Wang
Journal:  Org Lett       Date:  2014-07-17       Impact factor: 6.005

9.  Copper-catalyzed sulfonamides formation from sodium sulfinates and amines.

Authors:  Xiaodong Tang; Liangbin Huang; Chaorong Qi; Xia Wu; Wanqing Wu; Huanfeng Jiang
Journal:  Chem Commun (Camb)       Date:  2013-07-11       Impact factor: 6.222

10.  Synthesis of sulfones from organozinc reagents, DABSO, and alkyl halides.

Authors:  Benjamin N Rocke; Kevin B Bahnck; Michael Herr; Sophie Lavergne; Vincent Mascitti; Christian Perreault; Jana Polivkova; Andrei Shavnya
Journal:  Org Lett       Date:  2013-12-05       Impact factor: 6.005

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  99 in total

1.  Selective formation of heteroaryl thioethers via a phosphonium ion coupling reaction.

Authors:  Ryan G Anderson; Brianna M Jett; Andrew McNally
Journal:  Tetrahedron       Date:  2017-12-21       Impact factor: 2.457

2.  Synthesis, Antimicrobial and Antioxidant Activity of Pyrazole Based Sulfonamide Derivatives.

Authors:  Jagdish R Badgujar; Dhananjay H More; Jyotsna S Meshram
Journal:  Indian J Microbiol       Date:  2017-10-31       Impact factor: 2.461

3.  Monophosphine Ligands Promote Pd-Catalyzed C-S Cross-Coupling Reactions at Room Temperature with Soluble Bases.

Authors:  Jessica Xu; Richard Y Liu; Charles S Yeung; Stephen L Buchwald
Journal:  ACS Catal       Date:  2019-06-21       Impact factor: 13.084

4.  Sulfonamidation of Aryl and Heteroaryl Halides through Photosensitized Nickel Catalysis.

Authors:  Taehoon Kim; Stefan J McCarver; Chulbom Lee; David W C MacMillan
Journal:  Angew Chem Int Ed Engl       Date:  2018-02-27       Impact factor: 15.336

5.  Catalytic Hydrothiolation: Counterion-Controlled Regioselectivity.

Authors:  Xiao-Hui Yang; Ryan T Davison; Shao-Zhen Nie; Faben A Cruz; Tristan M McGinnis; Vy M Dong
Journal:  J Am Chem Soc       Date:  2019-02-08       Impact factor: 15.419

6.  Visible-Light-Promoted C-S Cross-Coupling via Intermolecular Charge Transfer.

Authors:  Bin Liu; Chern-Hooi Lim; Garret M Miyake
Journal:  J Am Chem Soc       Date:  2017-09-19       Impact factor: 15.419

Review 7.  Synthesis of sulfur-containing heterocycles via ring enlargement.

Authors:  Bakr F Abdel-Wahab; Saad Shaaban; Gamal A El-Hiti
Journal:  Mol Divers       Date:  2018-01-31       Impact factor: 2.943

8.  Dealkenylative Thiylation of C(sp3)-C(sp2) Bonds.

Authors:  Andrew J Smaligo; Ohyun Kwon
Journal:  Org Lett       Date:  2019-10-01       Impact factor: 6.005

Review 9.  Catalytic, Enantioselective Sulfenofunctionalization of Alkenes: Development and Recent Advances.

Authors:  Anastassia Matviitsuk; Jesse L Panger; Scott E Denmark
Journal:  Angew Chem Int Ed Engl       Date:  2020-08-18       Impact factor: 15.336

10.  RASS-Enabled S/P-C and S-N Bond Formation for DEL Synthesis.

Authors:  Dillon T Flood; Xuejing Zhang; Xiang Fu; Zhenxiang Zhao; Shota Asai; Brittany B Sanchez; Emily J Sturgell; Julien C Vantourout; Paul Richardson; Mark E Flanagan; David W Piotrowski; Dominik K Kölmel; Jinqiao Wan; Mei-Hsuan Tsai; Jason S Chen; Phil S Baran; Philip E Dawson
Journal:  Angew Chem Int Ed Engl       Date:  2020-03-11       Impact factor: 15.336

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