Literature DB >> 27043308

Stereoselective Total Synthesis of Bioactive Marine Natural Product Biselyngbyolide B.

Sayantan Das1, Debobrata Paul1, Rajib Kumar Goswami1.   

Abstract

A convergent strategy for the stereoselective total synthesis of biologically active marine natural product biselyngbyolide B has been developed. Key strategies of this synthesis include Jamison protocol of trans-hydroalumination/allylation for installation of C18-C23 olefin moiety and intramolecular Heck coupling for macrocyclization.

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Year:  2016        PMID： 27043308     DOI： 10.1021/acs.orglett.6b00713

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


  3 in total

1.  Total Synthesis of Cytospolide Q.

Authors:  Shamba Chatterjee; Gour Hari Mandal; Rajib Kumar Goswami
Journal:  ACS Omega       Date:  2018-07-05

Review 2.  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

3.  Total synthesis of nahuoic acid A via a putative biogenetic intramolecular Diels-Alder (IMDA) reaction.

Authors:  Lucía Guillade; Paula Mora; Pedro Villar; Rosana Alvarez; Angel R de Lera
Journal:  Chem Sci       Date:  2021-10-27       Impact factor: 9.825
  3 in total

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