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Volumn 61, Issue 11, 1996, Pages 3616-3622

Conversion of allylic alcohols into allylic nitromethyl compounds via a palladium-catalyzed solvolysis: An enantioselective synthesis of an advanced carbocyclic nucleoside precursor

Author keywords

[No Author keywords available]

Indexed keywords

CARBOCYCLIC NUCLEOSIDE;

EID: 0030007036     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo951510s     Document Type: Article
Times cited : (57)

References (40)
  • 1
    • 0000276556 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon; Oxford, U.K.
    • For a recent review see: Godleski, S. A. In Comprehensive Organic Syntheses; Trost, B. M., Fleming, I., Eds.; Pergamon; Oxford, U.K., 1991; Vol. 4, pp 585-661.
    • (1991) Comprehensive Organic Syntheses , vol.4 , pp. 585-661
    • Godleski, S.A.1
  • 2
    • 33751386697 scopus 로고
    • and references cited therein
    • Denmark, S. E.; Marcin, L. R. J. Org. Chem. 1993, 58, 3850 and references cited therein.
    • (1993) J. Org. Chem. , vol.58 , pp. 3850
    • Denmark, S.E.1    Marcin, L.R.2
  • 3
    • 0017919296 scopus 로고
    • Tsuji has reported the nucleophilic attack of nitroethane on the intermediate telomer complex derived from palladium and butadiene: Tsuji, J.; Yamakawa, T.; Mandai, T. Tetrahedron Lett. 1978, 565.
    • (1978) Tetrahedron Lett. , pp. 565
    • Tsuji, J.1    Yamakawa, T.2    Mandai, T.3
  • 18
    • 0001237911 scopus 로고
    • For similar approaches to carbocyclic nucleosides using "activated" nitromethyl derivatives see: (a) Peel, M. R.; Sternbach, D. D.; Johnson, M. R. J. Org. Chem. 1991, 56, 4990. (b) Trost, B. M.; Huo, G.; Benneche, T. J. Am. Chem. Soc. 1988, 110, 621.
    • (1991) J. Org. Chem. , vol.56 , pp. 4990
    • Peel, M.R.1    Sternbach, D.D.2    Johnson, M.R.3
  • 19
    • 0023850740 scopus 로고
    • For similar approaches to carbocyclic nucleosides using "activated" nitromethyl derivatives see: (a) Peel, M. R.; Sternbach, D. D.; Johnson, M. R. J. Org. Chem. 1991, 56, 4990. (b) Trost, B. M.; Huo, G.; Benneche, T. J. Am. Chem. Soc. 1988, 110, 621.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 621
    • Trost, B.M.1    Huo, G.2    Benneche, T.3
  • 23
    • 15844431645 scopus 로고    scopus 로고
    • Results from this study will be reported at a later date
    • Results from this study will be reported at a later date.
  • 26
    • 15844391093 scopus 로고    scopus 로고
    • Reference 16, p 62
    • Reference 16, p 62.
  • 27
    • 0024302311 scopus 로고
    • Matrix Presented
    • For accepted nomenclature for planar allyl ligands see: Consiglio, G.; Waymouth, R. M. Chem. Rev. 1989, 89, 257. (Matrix Presented)
    • (1989) Chem. Rev. , vol.89 , pp. 257
    • Consiglio, G.1    Waymouth, R.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.