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Synthesis of (3S*,4R*,6E,10Z)-3,4,7,11-tetramethyltrideca-6,10-dienal (faranal) using stereospecific 1,4-cis-hydrogenation of conjugated double bonds
Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
2000 (English)In: JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, ISSN 1470-4358, no 14, p. 2211-2216Article in journal (Refereed) Published
Abstract [en]

(+/-)-Faranal was synthesised by a convergent route involving 1,4-cis-hydrogenation of two properly substituted conjugated diene building blocks to introduce stereospecifically the 6(E) and 10(Z) double bonds of the final target molecule. meso-2,3-Dimethy

Place, publisher, year, edition, pages
ROYAL SOC CHEMISTRY , 2000. no 14, p. 2211-2216
Keyword [en]
TRAIL PHEROMONE; JUVENILE-HORMONE; ROUTE; ANT; COMPLEXES; ALCOHOLS; REAGENTS; ALUMINUM; ESTERS
Identifiers
URN: urn:nbn:se:uu:diva-37612OAI: oai:DiVA.org:uu-37612DiVA, id: diva2:65511
Note
Addresses: Serebryakov EP, Russian Acad Sci, ND Zelinskii Organ Chem Inst, Moscow 117913, Russia. Russian Acad Sci, ND Zelinskii Organ Chem Inst, Moscow 117913, Russia. Univ Uppsala, Dept Organ Chem, Inst Chem, S-75121 Uppsala, Sweden.Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2011-01-14

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