Literature DB >> 24096306

Construction of the basic skeleton of ophiobolin A and variecolin.

Ke Li1, Cheng Wang, Gang Yin, Shuanhu Gao.   

Abstract

Ophiobolin and variecolin type sesterterpenoids belong to cyclooctane-containing natural products. Both sesterterpenoids have challenging structures and appealing biological activities. We envisioned that a key tandem ring closing metathesis of dienynes could provide the basic skeleton of ophiobolin A and variecolin. We report herein the detailed reactivities of the dienynes which furnished the 5-8-5 and 5-8-6-5 rings efficiently.

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Year:  2013        PMID: 24096306     DOI: 10.1039/c3ob41693c

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


  3 in total

1.  Enantioselective synthesis of an ophiobolin sesterterpene via a programmed radical cascade.

Authors:  Zachary G Brill; Huck K Grover; Thomas J Maimone
Journal:  Science       Date:  2016-05-27       Impact factor: 47.728

2.  Total Synthesis of (+)-6-epi-Ophiobolin A.

Authors:  Danny Q Thach; Zachary G Brill; Huck K Grover; Kenneth V Esguerra; Jordan K Thompson; Thomas J Maimone
Journal:  Angew Chem Int Ed Engl       Date:  2019-12-12       Impact factor: 15.336

3.  Wolff/Cope Approach to the AB Ring of the Sesterterpenoid Variecolin.

Authors:  Michael R Krout; Christopher E Henry; Thomas Jensen; Kun-Liang Wu; Scott C Virgil; Brian M Stoltz
Journal:  J Org Chem       Date:  2018-01-23       Impact factor: 4.354

  3 in total

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