Literature DB >> 18563806

Diversity-oriented synthesis.

Richard J Spandl1, Mónica Díaz-Gavilán, Kieron M G O'Connell, Gemma L Thomas, David R Spring.   

Abstract

Diversity-oriented synthesis (DOS), which describes the synthesis of structurally diverse collections of small molecules, was developed, in part, to address combinatorial chemistry's shortfalls. In this paper, we hope to give an indication of what can be achieved using the DOS approach to library generation. We describe some of the most successful strategies utilized in DOS, with special focus on our own area of interest; DOS from simple, pluripotent starting materials. Copyright 2008 The Japan Chemical Journal Forum and Wiley Periodicals, Inc.

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Year:  2008        PMID: 18563806     DOI: 10.1002/tcr.20144

Source DB:  PubMed          Journal:  Chem Rec        ISSN: 1528-0691            Impact factor:   6.771


  11 in total

1.  Highly enantioselective dearomatizing formal [3+3] cycloaddition reactions of N-acyliminopyridinium ylides with electrophilic enol carbene intermediates.

Authors:  Xinfang Xu; Peter Y Zavalij; Michael P Doyle
Journal:  Angew Chem Int Ed Engl       Date:  2013-10-02       Impact factor: 15.336

2.  Combined electrochemical/chemical methods for the synthesis and the molecular diversifying of isoindolinone-based heterocyclic scaffolds.

Authors:  Laura Palombi; Antonia Di Mola; Chiara Vignes; Antonio Massa
Journal:  Mol Divers       Date:  2014-01-12       Impact factor: 2.943

3.  Diversity-oriented synthesis and antifungal activities of novel pimprinine derivative bearing a 1,3,4-oxadiazole-5-thioether moiety.

Authors:  Zi-Long Song; Yun Zhu; Jing-Rui Liu; Shu-Ke Guo; Yu-Cheng Gu; Xinya Han; Hong-Qiang Dong; Qi Sun; Wei-Hua Zhang; Ming-Zhi Zhang
Journal:  Mol Divers       Date:  2020-02-13       Impact factor: 2.943

4.  Automated synthesis of a 184-member library of thiadiazepan-1,1-dioxide-4-ones.

Authors:  Erik Fenster; Toby R Long; Qin Zang; David Hill; Benjamin Neuenswander; Gerald H Lushington; Aihua Zhou; Conrad Santini; Paul R Hanson
Journal:  ACS Comb Sci       Date:  2011-02-10       Impact factor: 3.784

5.  α-Haloarylsulfonamides: Multiple Cyclization Pathways to Skeletally Diverse Benzofused Sultams.

Authors:  Dinesh Kumar Rayabarapu; Aihua Zhou; Kyu Ok Jeon; Thiwanka Samarakoon; Alan Rolfe; Hina Siddiqui; Paul R Hanson
Journal:  Tetrahedron       Date:  2009-04-18       Impact factor: 2.457

6.  Synthesis of an Isoindoline-Annulated, Tricyclic Sultam Library via Microwave-Assisted, Continuous-Flow Organic Synthesis (MACOS).

Authors:  Farman Ullah; Qin Zang; Salim Javed; Patrick Porubsky; Benjamin Neuenswander; Gerald H Lushington; Paul R Hanson; Michael G Organ
Journal:  Synthesis (Stuttg)       Date:  2012       Impact factor: 3.157

7.  Two-directional synthesis as a tool for diversity-oriented synthesis: Synthesis of alkaloid scaffolds.

Authors:  Kieron M G O'Connell; Monica Díaz-Gavilán; Warren R J D Galloway; David R Spring
Journal:  Beilstein J Org Chem       Date:  2012-06-06       Impact factor: 2.883

Review 8.  Challenges and perspectives of chemical biology, a successful multidisciplinary field of natural sciences.

Authors:  Fernando A Rojas-Ruiz; Leonor Y Vargas-Méndez; Vladimir V Kouznetsov
Journal:  Molecules       Date:  2011-03-23       Impact factor: 4.411

9.  Ring-opening metathesis of some strained bicyclic systems; stereocontrolled access to diolefinated saturated heterocycles with multiple stereogenic centers.

Authors:  Zsanett Benke; Melinda Nonn; Márton Kardos; Santos Fustero; Loránd Kiss
Journal:  Beilstein J Org Chem       Date:  2018-10-24       Impact factor: 2.883

10.  Automated three-component synthesis of a library of γ-lactams.

Authors:  Erik Fenster; David Hill; Oliver Reiser; Jeffrey Aubé
Journal:  Beilstein J Org Chem       Date:  2012-10-19       Impact factor: 2.883

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