Literature DB >> 10602188

Total Synthesis of Everninomicin 13,384-1-Part 1: Synthesis of the A(1)B(A)C Fragment.

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Abstract

The powerful antibiotic everninomicin 13,384-1 (1, Ziracin) has been prepared for the first time through a total synthesis. The 1-->1'-disaccharide and the two orthoesters of this target molecule were introduced by new methodologies using a tin acetal and 1,2-phenylseleno migrations. The reaction sequence also relies on stereoselective glycosidations and subtle manipulations of protecting groups. In addition to the introduction of new synthetic methodologies, this total synthesis should allow the preparation of combinatorial libraries of semisynthetic analogues of this highly promising antibiotic for biological screening purposes.

Entities:  

Year:  1999        PMID: 10602188

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  5 in total

1.  Multiple-stage mass spectrometric analysis of complex oligosaccharide antibiotics (everninomicins) in a quadrupole ion trap.

Authors:  Guodong Chen; Birendra N Pramanik; Peter L Bartner; Anil K Saksena; Michael L Gross
Journal:  J Am Soc Mass Spectrom       Date:  2002-11       Impact factor: 3.109

Review 2.  Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance.

Authors:  K C Nicolaou; Christopher R H Hale; Christian Nilewski; Heraklidia A Ioannidou
Journal:  Chem Soc Rev       Date:  2012-06-28       Impact factor: 54.564

Review 3.  A brief history of antibiotics and select advances in their synthesis.

Authors:  Kyriacos C Nicolaou; Stephan Rigol
Journal:  J Antibiot (Tokyo)       Date:  2017-07-05       Impact factor: 2.649

4.  An efficient and cost-effective preparation of di-O-acetyl-D-rhamnal.

Authors:  Justin N Miller; Rongson Pongdee
Journal:  Tetrahedron Lett       Date:  2013-06-12       Impact factor: 2.415

5.  D-Glucose and D-mannose-based metabolic probes. Part 3: Synthesis of specifically deuterated D-glucose, D-mannose, and 2-deoxy-D-glucose.

Authors:  Izabela Fokt; Stanislaw Skora; Charles Conrad; Timothy Madden; Mark Emmett; Waldemar Priebe
Journal:  Carbohydr Res       Date:  2012-12-13       Impact factor: 2.104

  5 in total

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