Literature DB >> 17387656

Total synthesis of peribysin E necessitates revision of the assignment of its absolute configuration.

Angie R Angeles1, David C Dorn, Cynthia A Kou, Malcolm A S Moore, Samuel J Danishefsky.   

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Year:  2007        PMID: 17387656     DOI: 10.1002/anie.200604308

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


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  7 in total

Review 1.  Terpenes from marine-derived fungi.

Authors:  Rainer Ebel
Journal:  Mar Drugs       Date:  2010-08-13       Impact factor: 5.118

2.  Total synthesis of aspeverin via an iodine(III)-mediated oxidative cyclization.

Authors:  Adam M Levinson
Journal:  Org Lett       Date:  2014-08-29       Impact factor: 6.005

3.  Permuting Diels-Alder and Robinson Annulation Stereopatterns.

Authors:  Feng Peng; Mingji Dai; Angie R Angeles; Samuel J Danishefsky
Journal:  Chem Sci       Date:  2012-08-01       Impact factor: 9.825

4.  Total syntheses of (+)- and (-)-peribysin E.

Authors:  Angie R Angeles; Stephen P Waters; Samuel J Danishefsky
Journal:  J Am Chem Soc       Date:  2008-09-11       Impact factor: 15.419

5.  Synthesis of the tetracyclic core of Illicium sesquiterpenes using an organocatalyzed asymmetric Robinson annulation.

Authors:  Lynnie Trzoss; Jing Xu; Michelle H Lacoske; Emmanuel A Theodorakis
Journal:  Beilstein J Org Chem       Date:  2013-06-12       Impact factor: 2.883

Review 6.  Naturally occurring cell adhesion inhibitors.

Authors:  Satoshi Takamatsu
Journal:  J Nat Med       Date:  2018-05-19       Impact factor: 2.343

Review 7.  Recent Achievements in Total Synthesis for Integral Structural Revisions of Marine Natural Products.

Authors:  Min Woo Ha; Jonghoon Kim; Seung-Mann Paek
Journal:  Mar Drugs       Date:  2022-02-25       Impact factor: 5.118

  7 in total

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