Literature DB >> 21692467

A formal synthesis of SCH 351448.

Heekwang Park1, Hyoungsu Kim, Jiyong Hong.   

Abstract

An efficient formal synthesis of SCH 351448 was accomplished through the tandem cross-metathesis (CM)/oxa-Michael, the 1,4-syn aldol, the tandem oxidation/oxa-Michael, and the Suzuki coupling reaction.
© 2011 American Chemical Society

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Year:  2011        PMID： 21692467     DOI： 10.1021/ol201426c

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


  5 in total

1.  Total synthesis of (+)-SCH 351448.

Authors:  Kaicheng Zhu; James S Panek
Journal:  Org Lett       Date:  2011-08-11       Impact factor: 6.005

2.  Synthesis of a Library of 1,5,2-Dithiazepine 1,1-Dioxides. Part 1: A One-Pot Sulfonylation/Thia-Michael Protocol.

Authors:  Qin Zang; Aihua Zhou; Salim Javed; Pradip K Maity; Chris A Knudtson; Danse Bi; Jared J Hastings; Fatima Z Basha; Paul R Hanson
Journal:  Heterocycles       Date:  2012-12-31       Impact factor: 0.831

3.  Total Synthesis of (+)-SCH 351448: Efficiency via Chemoselectivity and Redox-Economy Powered by Metal Catalysis.

Authors:  Gang Wang; Michael J Krische
Journal:  J Am Chem Soc       Date:  2016-06-23       Impact factor: 15.419

4.  Total Synthesis of Clavosolide A via Tandem Allylic Oxidation/Oxa-Conjugate Addition Reaction.

Authors:  Joseph B Baker; Hyoungsu Kim; Jiyong Hong
Journal:  Tetrahedron Lett       Date:  2015-06-03       Impact factor: 2.415

5.  Synthesis of α,α'-trans-oxepanes through an organocatalytic oxa-conjugate addition reaction.

Authors:  Megan L Lanier; Amanda C Kasper; Hyoungsu Kim; Jiyong Hong
Journal:  Org Lett       Date:  2014-04-11       Impact factor: 6.005
  5 in total

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