Literature DB >> 11559187

New diterpenes from the Caribbean sponge Epipolasis reiswigi.

A D Rodríguez1, B Vera.   

Abstract

Two diterpenes, epipolone (1) and epipolol (3), produced by terpenoid pathways leading to a tricarbocyclic structure with an irregular "head to tail" isoprene configuration, have been isolated from the Caribbean marine sponge Epipolasis reiswigi collected in Puerto Rico. The structures of 1 and 3 were elucidated largely by 1D and 2D NMR methods and chemical conversion.

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Year:  2001        PMID: 11559187     DOI: 10.1021/jo0104734

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  A unified approach to the daucane and sphenolobane bicyclo[5.3.0]decane core: enantioselective total syntheses of daucene, daucenal, epoxydaucenal B, and 14-para-anisoyloxydauc-4,8-diene.

Authors:  Nathan B Bennett; Brian M Stoltz
Journal:  Chemistry       Date:  2013-12-02       Impact factor: 5.236

2.  Four New Pregnane-10,2-carbolactones from an Epipolasis sp. Marine Sponge.

Authors:  Unwoo Kang; Dongdong Wang; Heidi R Bokesch; Kirk R Gustafson
Journal:  Chem Pharm Bull (Tokyo)       Date:  2021       Impact factor: 1.903

  2 in total

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