Literature DB >> 20625592

Formal synthesis of platencin.

Pingfan Li1, Hisashi Yamamoto.   

Abstract

Formal synthesis of platencin was achieved by assembling its tricyclic core structure through a Robinson annulation reaction, whose precursor was made from a bicyclo[3.2.2] ring structure, product of a tropone Diels-Alder reaction.

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Year:  2010        PMID： 20625592     DOI： 10.1039/c0cc01619e

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


  5 in total

Review 1.  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 2.  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

3.  Short Enantioselective Formal Synthesis of (-)-Platencin.

Authors:  Christian Defieber; Justin T Mohr; Gennadii A Grabovyi; Brian M Stoltz
Journal:  Synthesis (Stuttg)       Date:  2018-07-23       Impact factor: 3.157

4.  Organocatalytic stereoselective [8+2] and [6+4] cycloadditions.

Authors:  Rasmus Mose; Gert Preegel; Jesper Larsen; Sofie Jakobsen; Eva Høgh Iversen; Karl Anker Jørgensen
Journal:  Nat Chem       Date:  2016-12-19       Impact factor: 24.427

5.  Ni(NHC)]-catalyzed cycloaddition of diynes and tropone: apparent enone cycloaddition involving an 8π insertion.

Authors:  Puneet Kumar; Ashish Thakur; Xin Hong; K N Houk; Janis Louie
Journal:  J Am Chem Soc       Date:  2014-12-05       Impact factor: 15.419
  5 in total

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