By the same authors

From the same journal

A NEW ROUTE TO TRIENALS USING 2-SUBSTITUTED 2H-PYRAN-BASED WITTIG REAGENTS

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Publication details

JournalJOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS
DatePublished - 21 Sep 1993
Issue number18
Number of pages2
Pages (from-to)1409-1410
Original languageEnglish

Abstract

A procedure is presented which allows the six-carbon homologation of aldehydes to give the corresponding trienals via the likely intermediacy of the novel 2-triphenylphosphoranylidenemethyl-2H-pyran; application of this methodology to a short synthesis of the marine alarm pheromone, navenone B, is also described.

    Research areas

  • STEREOSELECTIVE SYNTHESIS, ORGANOMETALLIC REAGENTS, LTB4

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