Literature DB >> 21559534

De novo synthesis of natural products via the asymmetric hydration of polyenes.

Yanping Wang1, Yalan Xing, Qi Zhang, George A O'Doherty.   

Abstract

For the last ten years our group has been working toward the development of an asymmetric hydration approach to polyketide natural products based on the regioselective hydration of di- and tri-enoates. Key to the success of this approach is the recognition that both high regiocontrol and asymmetric induction could be obtained by the use of a Sharpless asymmetric dihydroxylation reaction. Herein we describe the development of the method and its application to natural product total synthesis. This journal is © The Royal Society of Chemistry 2011

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Year:  2011        PMID: 21559534      PMCID: PMC5815319          DOI: 10.1039/c1cc11791b

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  101 in total

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Authors:  T J Hunter; G A O'Doherty
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5.  An enantioselective synthesis of cryptocarya diacetate.

Authors:  T J Hunter; G A O'Doherty
Journal:  Org Lett       Date:  2001-08-23       Impact factor: 6.005

6.  A total synthesis of tarchonanthuslactone exploiting N-pyrrole carbinols as efficient stereocontrolling elements.

Authors:  Mark S Scott; Chris A Luckhurst; Darren J Dixon
Journal:  Org Lett       Date:  2005-12-22       Impact factor: 6.005

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Authors:  D Balachari; G A O'Doherty
Journal:  Org Lett       Date:  2000-03-23       Impact factor: 6.005

8.  Asymmetric total synthesis of (+)-phoslactomycin B.

Authors:  Setsuya Shibahara; Masataka Fujino; Yasumasa Tashiro; Keisuke Takahashi; Jun Ishihara; Susumi Hatakeyama
Journal:  Org Lett       Date:  2008-05-08       Impact factor: 6.005

9.  De novo synthesis of the trisaccharide subunit of landomycins A and E.

Authors:  Maoquan Zhou; George A O'Doherty
Journal:  Org Lett       Date:  2008-05-08       Impact factor: 6.005

10.  Strategy for enantio- and diastereoselective syntheses of all possible stereoisomers of 1,3-polyol arrays based on a highly catalyst-controlled epoxidation of alpha,beta-unsaturated morpholinyl amides: application to natural product synthesis.

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Journal:  Chemistry       Date:  2004-03-19       Impact factor: 5.236

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Journal:  Angew Chem Int Ed Engl       Date:  2012-04-05       Impact factor: 15.336

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  3 in total

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