Literature DB >> 18027960

Synthetic study of diversifolin: the construction of 11-oxabicyclo[6.2.1]undec-3-ene core using ring-closing metathesis.

Tomoaki Nakamura1, Motoko Oshida, Tomoko Nomura, Atsuo Nakazaki, Susumu Kobayashi.   

Abstract

Stereoselective synthesis of a potential intermediate bearing 11-oxabicyclo[6.2.1]undec-3-ene core, a common scaffold of biologically active germacrane-type sesquiterpenes, has been achieved. Synthetic features involve formal 1,3-asymmetric induction, unusual ring-closing metathesis constructing a 10-membered carbocycle system, and unique lactone transposition.

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Year:  2007        PMID: 18027960     DOI: 10.1021/ol7025119

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


  1 in total

Review 1.  Synthetic explorations of the briarane jungle: progress in developing a synthetic route to a common family of diterpenoid natural products.

Authors:  Nicholas G Moon; Andrew M Harned
Journal:  R Soc Open Sci       Date:  2018-05-23       Impact factor: 2.963

  1 in total

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