Literature DB >> 16268569

A convergent total synthesis of ustiloxin D via an unprecedented copper-catalyzed ethynyl aziridine ring-opening by phenol derivatives.

Pixu Li1, Cory D Evans, Madeleine M Joullié.   

Abstract

[reaction: see text] The ustiloxins are a family of heterodetic cyclopeptides that have been isolated from the water extracts of false smut balls on the panicles of rice plants caused by the fungus Ustilaginoidea virens. A concise total synthesis of ustiloxin D has been achieved via an unprecedented ethynyl aziridine ring-opening of phenol derivatives. The longest linear sequence of the synthesis is 15 steps from commercially available compounds.

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Year:  2005        PMID: 16268569     DOI: 10.1021/ol052287g

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  5 in total

1.  The enantioselective synthesis of phomopsin B.

Authors:  Joshua S Grimley; Andrew M Sawayama; Hiroko Tanaka; Michelle M Stohlmeyer; Thomas F Woiwode; Thomas J Wandless
Journal:  Angew Chem Int Ed Engl       Date:  2007       Impact factor: 15.336

2.  Structure-activity relationships of ustiloxin analogues.

Authors:  Madeleine M Joullié; Simon Berritt; Ernest Hamel
Journal:  Tetrahedron Lett       Date:  2011-04       Impact factor: 2.415

3.  Ring-opening of aziridine-2-carboxamides with carbohydrate C1-O-nucleophiles. Stereoselective preparation of alpha- and beta-O-glycosyl serine conjugates.

Authors:  Daniel A Ryan; David Y Gin
Journal:  J Am Chem Soc       Date:  2008-10-25       Impact factor: 15.419

4.  Evolution of the total syntheses of ustiloxin natural products and their analogues.

Authors:  Pixu Li; Cory D Evans; Yongzhong Wu; Bin Cao; Ernest Hamel; Madeleine M Joullié
Journal:  J Am Chem Soc       Date:  2008-01-30       Impact factor: 15.419

5.  Total synthesis of the reported structure of ceanothine D via a novel macrocyclization strategy.

Authors:  Jisun Lee; Madeleine M Joullié
Journal:  Chem Sci       Date:  2018-01-31       Impact factor: 9.825

  5 in total

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