Literature DB >> 23620262

Biological stereoselectivity of atropisomeric natural products and drugs.

Arie Zask1, John Murphy, George A Ellestad.   

Abstract

Selected examples of natural product and drug atropisomers that exhibit stereoselectivity towards receptor and enzyme targets are reviewed. The atropisomeric preference of the receptors and enzyme binding domains makes these agents attractive molecules for drug development in the treatment of various diseases. Included are commonly recognized atropisomers containing a chiral biaryl axis along with some less common examples of atropisomers without a biaryl axis. The biological targets include: antiapoptotic proteins; bacteria; microtubules; kinases; vasopressin receptors; a G-protein coupled receptor related to obesity; monocarboxylate transporters; tachykinin NK1 -receptors; cyclooxygenase-1 and squalene synthase.
Copyright © 2013 Wiley Periodicals, Inc.

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Year:  2013        PMID: 23620262     DOI: 10.1002/chir.22145

Source DB:  PubMed          Journal:  Chirality        ISSN: 0899-0042            Impact factor:   2.437


  22 in total

1.  Symmetry in Cascade Chirality-Transfer Processes: A Catalytic Atroposelective Direct Arylation Approach to BINOL Derivatives.

Authors:  Jin-Zheng Wang; Jin Zhou; Chang Xu; Hongbin Sun; László Kürti; Qing-Long Xu
Journal:  J Am Chem Soc       Date:  2016-04-14       Impact factor: 15.419

2.  A microchip electrophoresis-mass spectrometric platform for fast separation and identification of enantiomers employing the partial filling technique.

Authors:  Xiangtang Li; Dan Xiao; Xiao-Ming Ou; Cassandra McCullm; Yi-Ming Liu
Journal:  J Chromatogr A       Date:  2013-11-29       Impact factor: 4.759

Review 3.  Atropisomerism in medicinal chemistry: challenges and opportunities.

Authors:  Sean T Toenjes; Jeffrey L Gustafson
Journal:  Future Med Chem       Date:  2018-01-30       Impact factor: 3.808

4.  Catalytic enantioselective synthesis of atropisomeric biaryls by a cation-directed O-alkylation.

Authors:  John D Jolliffe; Roly J Armstrong; Martin D Smith
Journal:  Nat Chem       Date:  2017-01-23       Impact factor: 24.427

5.  Enantioselective Synthesis of Pyrrolopyrimidine Scaffolds through Cation-Directed Nucleophilic Aromatic Substitution.

Authors:  Mariel M Cardenas; Sean T Toenjes; Christopher J Nalbandian; Jeffrey L Gustafson
Journal:  Org Lett       Date:  2018-03-21       Impact factor: 6.005

6.  Troponoid Atropisomerism: Studies on the Configurational Stability of Tropone-Amide Chiral Axes.

Authors:  Danielle R Hirsch; Anthony J Metrano; Elizabeth A Stone; Golo Storch; Scott J Miller; Ryan P Murelli
Journal:  Org Lett       Date:  2019-03-14       Impact factor: 6.005

7.  Computationally Assisted Mechanistic Investigation and Development of Pd-Catalyzed Asymmetric Suzuki-Miyaura and Negishi Cross-Coupling Reactions for Tetra-ortho-Substituted Biaryl Synthesis.

Authors:  Nitinchandra Dahyabhai Patel; Joshua D Sieber; Sergei Tcyrulnikov; Bryan J Simmons; Daniel Rivalti; Krishnaja Duvvuri; Yongda Zhang; Donghong A Gao; Keith R Fandrick; Nizar Haddad; Kendricks So Lao; Hari Prasad Reddy Mangunuru; Soumik Biswas; Bo Qu; Nelu Grinberg; Scott Pennino; Heewon Lee; Jinhua J Song; B Frank Gupton; Neil K Garg; Marisa C Kozlowski; Chris H Senanayake
Journal:  ACS Catal       Date:  2018-09-20       Impact factor: 13.084

8.  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

9.  Practical Organocatalytic Synthesis of Functionalized Non-C2-Symmetrical Atropisomeric Biaryls.

Authors:  Hongyin Gao; Qing-Long Xu; Craig Keene; Muhammed Yousufuddin; Daniel H Ess; László Kürti
Journal:  Angew Chem Int Ed Engl       Date:  2015-11-23       Impact factor: 15.336

10.  Synthesis of enantiomerically pure helicene like bis-oxazines from atropisomeric 7,7'-dihydroxy BINOL: Preliminary measurements of the circularly polarized luminescence.

Authors:  M Shyam Sundar; Harish R Talele; Hemant M Mande; Ashutosh V Bedekar; Roberto C Tovar; Gilles Muller
Journal:  Tetrahedron Lett       Date:  2014-03-01       Impact factor: 2.415

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