Literature DB >> 16032344

A comparative analysis of the total syntheses of the amphidinolide T natural products.

Elizabeth A Colby1, Timothy F Jamison.   

Abstract

In this article we compare and contrast the strategies and tactics used in the syntheses of the amphidinolide T family of natural products that have been reported by Fürstner, Ghosh and ourselves. Similar approaches to the trisubstituted THF ring present in the targets are utilized in all of the syntheses, but each strategy showcases a different means of macrocyclization.

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Year:  2005        PMID: 16032344     DOI: 10.1039/b507315b

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  4 in total

1.  Amphidinolide B: total synthesis, structural investigation, and biological evaluation.

Authors:  Liang Lu; Wei Zhang; Sangkil Nam; David A Horne; Richard Jove; Rich G Carter
Journal:  J Org Chem       Date:  2013-02-13       Impact factor: 4.354

2.  Regioselectivity and enantioselectivity in nickel-catalysed reductive coupling reactions of alkynes.

Authors:  Ryan M Moslin; Karen Miller-Moslin; Timothy F Jamison
Journal:  Chem Commun (Camb)       Date:  2007-07-03       Impact factor: 6.222

3.  Exploiting hidden symmetry in natural products: total syntheses of amphidinolides C and F.

Authors:  Subham Mahapatra; Rich G Carter
Journal:  J Am Chem Soc       Date:  2013-07-11       Impact factor: 15.419

Review 4.  Unconventional Macrocyclizations in Natural Product Synthesis.

Authors:  Iakovos Saridakis; Daniel Kaiser; Nuno Maulide
Journal:  ACS Cent Sci       Date:  2020-09-21       Impact factor: 14.553

  4 in total

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