Literature DB >> 17979279

New efficient route to an advanced precursor of the AB spiroketal of spongistatins.

Sylvain Favre1, Sandrine Gerber-Lemaire, Pierre Vogel.   

Abstract

A sequence of highly diastereoselective functionalizations allowed transformation of a meso-methylenebis(cyclohept-3-ene-1,6-diyl diester) into an advanced precursor of the AB spiroketal of spongistatins. This route illustrates the potential of this bis-cycloheptene derivative for the synthesis of a key fragment of complex bioactive natural compounds.

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Year:  2007        PMID: 17979279     DOI: 10.1021/ol702326x

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


  3 in total

1.  Total synthesis of auripyrone A using a tandem non-aldol aldol/Paterson aldol process as a key step.

Authors:  Michael E Jung; Ramin Salehi-Rad
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

2.  Catalytic asymmetric synthesis of geminal-dicarboxylates.

Authors:  Nisha Mistry; Stephen P Fletcher
Journal:  Chem Sci       Date:  2018-06-28       Impact factor: 9.825

Review 3.  Recent synthetic approaches toward non-anomeric spiroketals in natural products.

Authors:  Sylvain Favre; Pierre Vogel; Sandrine Gerber-Lemaire
Journal:  Molecules       Date:  2008       Impact factor: 4.411

  3 in total

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