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Alternative synthesis of trans-8,10-dimethyl-1(9)-octal-2-one

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    Alternative synthesis of trans-8,10-dimethyl-1(9)-octal-2-one
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    The Journal of Organic Chemistry

    Cite this: J. Org. Chem. 1969, 34, 1, 222–224
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    https://doi.org/10.1021/jo00838a049
    Published January 1, 1969
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    This article is cited by 19 publications.

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    2. Richard C. Larock, Li Zhang. Formation of Alkynes by Isomerization and Metathesis. 2018, 1-6. https://doi.org/10.1002/9781118662083.cot03-001
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    5. Florian Gallier, Arnaud Martel, Gilles Dujardin. Enantioselective Access to Robinson Annulation Products and Michael Adducts as Precursors. Angewandte Chemie International Edition 2017, 56 (41) , 12424-12458. https://doi.org/10.1002/anie.201701401
    6. Olga Konstantinova, Florence C.E. Sarabèr, Enrique Melguizo, Ben J.M. Jansen, Aede de Groot. 1-Phenylthio-3-vinyl-3-cyclohexenol, a new reagent for bis-annelation of silyl enol ethers. Tetrahedron 2006, 62 (8) , 1749-1755. https://doi.org/10.1016/j.tet.2005.11.060
    7. Valsamma Varghese, Manasi Saha, Kenneth M. Nicholas. Alkylations Using Hexacarbonyl(Propargylium)Dicobalt Salts: 2‐(1‐Methyl‐2‐Propynyl)Cyclohexanone. 2003, 141-141. https://doi.org/10.1002/0471264180.os067.18
    8. Raymond E. Conrow. 1,3-Dichloro-2-butene. 2001https://doi.org/10.1002/047084289X.rd111
    9. Mitsuhiro Yoshimatsu, Hiroshi Shimizu, Tadashi Kataoka. A reaction of γ-chalcogen-substituted prop-2-ynyl cations with mild nucleophiles. J. Chem. Soc., Chem. Commun. 1995, 101 (2) , 149-150. https://doi.org/10.1039/C39950000149
    10. R. van der Steen, P. L. Biesheuvel, J. Lugtenburg, C. Erkelens, R. A. Mathies. 8,16‐ And 8,18‐methanobacteriorhodopsin. Synthesis and spectroscopy of 8,16‐ and 8,18‐methanoretinal and their interaction with bacterioopsin. Recueil des Travaux Chimiques des Pays-Bas 1989, 108 (3) , 83-93. https://doi.org/10.1002/recl.19891080302
    11. Uwe Bunz, Günter Szeimies. Synthesis of 1-alkynylbicyclo[1.1.1]pentanes. Tetrahedron Letters 1989, 30 (16) , 2087-2088. https://doi.org/10.1016/S0040-4039(01)93718-9
    12. P. Duhamel, L. Hennequin, J.M. Poirier, G. Tavel, C. Vottero. 1,5-Dicarbonyl compounds. Tetrahedron 1986, 42 (17) , 4777-4786. https://doi.org/10.1016/S0040-4020(01)82058-5
    13. Robert K. Boeckman. The utility of silicon in organic synthesis. Tetrahedron 1983, 39 (6) , 925-934. https://doi.org/10.1016/S0040-4020(01)88591-4
    14. L. M. Browne, R. E. Klinck, J. B. Stothers. Carbon‐13 NMR Studies: 82. Carbon‐13 spectra of several 10‐methyl‐ cis ‐decalins. Conformational preferences of some cis ‐decalin derivatives. Organic Magnetic Resonance 1979, 12 (10) , 561-568. https://doi.org/10.1002/mrc.1270121004
    15. Makoto Kobayashi, Takeshi Matsumoto. Modifizierte Wichterle-Reaktion. Ein Weg zur Darstellung von 2-Cyclohexenonen und 1,4-Diketonen. Synthese von 4-Estren-3,17-dion und Dihydrojasmon. Bulletin of the Chemical Society of Japan 1979, 52 (10) , 2978-2990. https://doi.org/10.1246/bcsj.52.2978
    16. Robert Ramage. Synthesis of Sesquiterpenoids of Biogenetic Importance. 1978, 67-83. https://doi.org/10.1002/9780470720349.ch6
    17. Michael E. Jung. A review of annulation. Tetrahedron 1976, 32 (1) , 3-31. https://doi.org/10.1016/0040-4020(76)80016-6
    18. B. Maurer, M. Fracheboud, A. Grieder, G. Ohloff. Zur Kenntnis der sesquiterpenoiden C 12 ‐Ketone des ätherischen Öls von Vetiveria zizanioides (L.) Nash. Helvetica Chimica Acta 1972, 55 (7) , 2371-2382. https://doi.org/10.1002/hlca.19720550712
    19. D. Becker, J. Kalo. A new approach to the synthesis of 4,4-disubstituted -2-cyclohexenone. Tetrahedron Letters 1971, 12 (40) , 3725-3726. https://doi.org/10.1016/0040-4039(71)80012-6
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    The Journal of Organic Chemistry

    Cite this: J. Org. Chem. 1969, 34, 1, 222–224
    Click to copy citationCitation copied!
    https://doi.org/10.1021/jo00838a049
    Published January 1, 1969
    Request reuse permissions

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