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Volumn 47, Issue 22, 2008, Pages 4184-4187

Diastereoselective tetrahydropyrone synthesis through transition-metal-free oxidative carbon-hydrogen bond activation

Author keywords

C H activation; Cyclization; Oxidation; Substituent effects; Synthetic methods

Indexed keywords

BINDING SITES; CHEMICAL BONDS; CHEMICAL REACTIONS; CYCLIZATION; ETHERS; FUNCTIONAL GROUPS; HYDROGEN; ORGANIC COMPOUNDS; POSITIVE IONS; SYNTHESIS (CHEMICAL); TRANSITION METALS;

EID: 47049107187     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200706002     Document Type: Article
Times cited : (111)

References (48)
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    • For reviews of radical cation reactivity patterns, see; a
    • For reviews of radical cation reactivity patterns, see; a) M. Schmittel, A. Burghart, Angew. Chem. 1997, 109, 2658;
    • (1997) Angew. Chem , vol.109 , pp. 2658
    • Schmittel, M.1    Burghart, A.2
  • 22
    • 0040553331 scopus 로고
    • For other examples of carbon-carbon bond formation through ether oxidation, see: a
    • For other examples of carbon-carbon bond formation through ether oxidation, see: a) T. Mukaiyama, H. Nagaoka, M. Ohshima, M. Murakami, Chem. Lett. 1986, 1009;
    • (1986) Chem. Lett , pp. 1009
    • Mukaiyama, T.1    Nagaoka, H.2    Ohshima, M.3    Murakami, M.4
  • 34
    • 0000751061 scopus 로고    scopus 로고
    • For discussions of the stereoelectronic requirements for efficient bond cleavage reactions of radical cations, see: a L. M. Tolbert, R. K. Khanna, A. E. Popp, L. Gelbaum, L. A. Bottomley, J. Am. Chem. Soc. 1990, 112, 2373;
    • For discussions of the stereoelectronic requirements for efficient bond cleavage reactions of radical cations, see: a) L. M. Tolbert, R. K. Khanna, A. E. Popp, L. Gelbaum, L. A. Bottomley, J. Am. Chem. Soc. 1990, 112, 2373;
  • 38
    • 53549112577 scopus 로고    scopus 로고
    • -1. D. F. McMillen, D. M. Golden, Annu. Rev. Phys. Chem. 1982, 33, 493.
    • -1. D. F. McMillen, D. M. Golden, Annu. Rev. Phys. Chem. 1982, 33, 493.
  • 45
    • 53549103667 scopus 로고    scopus 로고
    • The origin of this curious but useful effect has not been elucidated
    • The origin of this curious but useful effect has not been elucidated.
  • 48
    • 0037043188 scopus 로고    scopus 로고
    • Oxidative prenyl ether cleavage has been shown to be faster than allyl ether cleavage. J. M. Vatèle, Tetrahedron 2002, 58, 5689.
    • Oxidative prenyl ether cleavage has been shown to be faster than allyl ether cleavage. J. M. Vatèle, Tetrahedron 2002, 58, 5689.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.