A simple method for the conversion of primary alcohols into terminal olefins

Chemistry Letters

Volumn , Issue 12, 1996, Pages 1039-1040

  Matsushita, Masayuki ^a   Nagaoka, Yoko ^a   Hioki, Hideaki ^a   Fukuyama, Yoshiyasu ^a   Kodama, Mitsuaki ^a  

^a TOKUSHIMA BUNRI UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 1542535886     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.1996.1039     Document Type: Article

References (10)

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2. K. Laali, R. J. Gerzina, C. M. Flajnik, C. M. Geric, and A. M. Dombroski, Helv. Chim. Acta., 70, 607 (1987). G. J. Cernigliaro and P. J. Kocienski, J. Org. Chem., 42, 3622 (1977).
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5. For reviews on [1,2]-and [2,3]-Wittig rearrangement, see: U. Schöllkopf, Angew. Chem., 82, 795 (1970). Angew. Chem., Int. Ed. Eng., 9, 763 (1970). T. Nakai and K. Mikami, Chem Rev., 86, 885 (1986). J. A. Marshall, in "Comprehensive Organic Synthesis," ed by G. Pattenden, Pergamon Press, London (1991), Vol. 3, p. 975.
6. For reviews on [1,2]-and [2,3]-Wittig rearrangement, see: U. Schöllkopf, Angew. Chem., 82, 795 (1970). Angew. Chem., Int. Ed. Eng., 9, 763 (1970). T. Nakai and K. Mikami, Chem Rev., 86, 885 (1986). J. A. Marshall, in "Comprehensive Organic Synthesis," ed by G. Pattenden, Pergamon Press, London (1991), Vol. 3, p. 975.
7. For reviews on [1,2]-and [2,3]-Wittig rearrangement, see: U. Schöllkopf, Angew. Chem., 82, 795 (1970). Angew. Chem., Int. Ed. Eng., 9, 763 (1970). T. Nakai and K. Mikami, Chem Rev., 86, 885 (1986). J. A. Marshall, in "Comprehensive Organic Synthesis," ed by G. Pattenden, Pergamon Press, London (1991), Vol. 3, p. 975.
8. For reviews on [1,2]-and [2,3]-Wittig rearrangement, see: U. Schöllkopf, Angew. Chem., 82, 795 (1970). Angew. Chem., Int. Ed. Eng., 9, 763 (1970). T. Nakai and K. Mikami, Chem Rev., 86, 885 (1986). J. A. Marshall, in "Comprehensive Organic Synthesis," ed by G. Pattenden, Pergamon Press, London (1991), Vol. 3, p. 975.
9. C. R. Hauser and S. W. Kantor, J. Am. Chem. Soc., 73, 1437 (1951).
10. It has long been known that organolithium decomposes diethyl ether to ethylene and lithium ethoxide. A. Maercker, Angew. Chem., Int. Ed. Eng., 26, 972 (1987). and reference sited herein.