Literature DB >> 20392661

Recent advances in multicomponent reactions for diversity-oriented synthesis.

James E Biggs-Houck1, Ashkaan Younai, Jared T Shaw.   

Abstract

Interest in multicomponent reactions (MCRs) has surged during the past two decades as interest in the efficient synthesis of small molecule libraries has gained prominence. MCRs fill an important niche in library synthesis by providing direct access to library compounds and by serving as starting points for Diversity-Oriented Synthesis (DOS). Recent advances in the area of MCR chemistry have included the discovery of new reactions, development of the first asymmetric catalysts, and the application of MCRs to natural products and other targets of biological interest. This review will highlight recent developments in MCRs as a rich source of molecular diversity. Copyright 2010 Elsevier Ltd. All rights reserved.

Mesh:

Substances:

Year:  2010        PMID: 20392661     DOI: 10.1016/j.cbpa.2010.03.003

Source DB:  PubMed          Journal:  Curr Opin Chem Biol        ISSN: 1367-5931            Impact factor:   8.822


  32 in total

1.  Three-component reactions of isocyanides, dialkyl acetylenedicarboxylates, and trans-cinnamoyl chlorides for the synthesis of highly functionalized 2-vinyl furans.

Authors:  Abbas Ali Esmaeili; Mahdieh Zangouei; Rahele Hosseinabadi; Ali Reza Fakhari
Journal:  Mol Divers       Date:  2011-12-16       Impact factor: 2.943

2.  Diversity-oriented synthesis as a tool for the discovery of novel biologically active small molecules.

Authors:  Warren R J D Galloway; Albert Isidro-Llobet; David R Spring
Journal:  Nat Commun       Date:  2010-09-21       Impact factor: 14.919

3.  Ammonia synthons for the multicomponent assembly of complex gamma-lactams.

Authors:  Darlene Q Tan; Kevin S Martin; James C Fettinger; Jared T Shaw
Journal:  Proc Natl Acad Sci U S A       Date:  2011-02-02       Impact factor: 11.205

4.  Synthesis of isoindolin-1-one derivatives via multicomponent reactions of methyl 2-formylbenzoate and intramolecular amidation.

Authors:  Jie Lei; Zhi-Gang Xu; Shi-Qiang Li; Jia Xu; Jin Zhu; Zhong-Zhu Chen
Journal:  Mol Divers       Date:  2016-06-07       Impact factor: 2.943

5.  New route for the synthesis of new cyanoimino- and cyanoaminopyrimidines.

Authors:  Amer Anwar Amer; Amr Hassan Moustafa
Journal:  Mol Divers       Date:  2017-07-10       Impact factor: 2.943

6.  A simple and efficient synthesis of fused morpholine pyrrolidines/piperdines with potential insecticidal activities.

Authors:  Jiayi Wang; Beiling Xu; Shanyu Si; Hui Li; Gonghua Song
Journal:  Mol Divers       Date:  2014-06-14       Impact factor: 2.943

7.  Expanding the substrate scope of Ugi five-center, four-component reaction U-5C-4CR): ketones as coupling partners for secondary amino acids.

Authors:  Maciej Dawidowski; Sławomir Sobczak; Marcin Wilczek; Artur Kulesza; Jadwiga Turło
Journal:  Mol Divers       Date:  2013-10-24       Impact factor: 2.943

8.  Three-component asymmetric catalytic Ugi reaction--concinnity from diversity by substrate-mediated catalyst assembly.

Authors:  Wenjun Zhao; Li Huang; Yong Guan; William D Wulff
Journal:  Angew Chem Int Ed Engl       Date:  2014-02-19       Impact factor: 15.336

9.  Synthesis of a library of "lead-like" γ-lactams by a one pot, four-component reaction.

Authors:  Kevin S Martin; Michael J Di Maso; James C Fettinger; Jared T Shaw
Journal:  ACS Comb Sci       Date:  2013-06-12       Impact factor: 3.784

10.  Multicomponent assembly of highly substituted indoles by dual palladium-catalyzed coupling reactions.

Authors:  John M Knapp; Jie S Zhu; Dean J Tantillo; Mark J Kurth
Journal:  Angew Chem Int Ed Engl       Date:  2012-09-24       Impact factor: 15.336

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.