Literature DB >> 18798670

Asymmetric synthesis of 6'-hydroxyarenarol: the proposed biosynthetic precursor to popolohuanone E.

Rachel H Munday1, Ross M Denton, James C Anderson.   

Abstract

The first synthesis of (+)-6'-hydroxyarenarol 3, the proposed biogenetic precursor to popolohuanone E (1), is described. An enantioselective route to key iodide intermediate 12 has been developed allowing the asymmetric synthesis of the known cis-decalin 22. Conditions which allow the removal of the methyl ether protecting groups on the hydroxyarene leaving the exocyclic methylene moiety in tact have also been developed to complete this synthesis.

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Year:  2008        PMID: 18798670     DOI: 10.1021/jo801404u

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


  3 in total

Review 1.  Cytotoxic terpene quinones from marine sponges.

Authors:  Marina Gordaliza
Journal:  Mar Drugs       Date:  2010-11-24       Impact factor: 5.118

2.  Synthesis, crystal structure and larvicidal activity of novel diamide derivatives against Culex pipiens.

Authors:  Rui Wu; Cong Zhu; Xiu-Jiang Du; Li-Xia Xiong; Shu-Jing Yu; Xing-Hai Liu; Zheng-Ming Li; Wei-Guang Zhao
Journal:  Chem Cent J       Date:  2012-09-11       Impact factor: 4.215

3.  General Methodologies Toward cis-Fused Quinone Sesquiterpenoids. Enantiospecific Synthesis of the epi-Ilimaquinone Core Featuring Sc-Catalyzed Ring Expansion.

Authors:  Hilan Z Kaplan; Victor L Rendina; Jason S Kingsbury
Journal:  Molecules       Date:  2017-06-24       Impact factor: 4.411

  3 in total

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