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Volumn 11, Issue 2, 2000, Pages 453-464

Stereoselective carbon-carbon bond forming reactions of chiral cyclopent-2-enone and cyclopentene-1-methanol, both spiro-connecting a 1,2:5,6-di-O-isopropylidene-α-D-glucofuranosyl ring

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPENTENE DERIVATIVE; CYCLOPENTENONE DERIVATIVE; MALONIC ACID DERIVATIVE; ORGANOMETALLIC COMPOUND; REAGENT;

EID: 0034635631     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(99)00490-5     Document Type: Article
Times cited : (8)

References (29)
  • 2
    • 0033597970 scopus 로고    scopus 로고
    • For a recent review on the synthesis of spirocyclic compounds, see
    • For a recent review on the synthesis of spirocyclic compounds, see: Sannigrahi, M. Tetrahedron 1999, 55, 9007-9071.
    • (1999) Tetrahedron , vol.55 , pp. 9007-9071
    • Sannigrahi, M.1
  • 8
    • 0032540434 scopus 로고    scopus 로고
    • For some total syntheses of natural products starting from 1 achieved recently in our laboratory, see: (a)
    • For some total syntheses of natural products starting from 1 achieved recently in our laboratory, see: (a) Ishihara, J.; Nonaka, R.; Terasawa, Y.; Shiraki, R.; Yabu, K.; Kataoka, H.; Ochiai, Y.; Tadano, K. J. Org. Chem. 1998, 63, 2679-2688.
    • (1998) J. Org. Chem. , vol.63 , pp. 2679-2688
    • Ishihara, J.1    Nonaka, R.2    Terasawa, Y.3    Shiraki, R.4    Yabu, K.5    Kataoka, H.6    Ochiai, Y.7    Tadano, K.8
  • 11
    • 0032509270 scopus 로고    scopus 로고
    • For highly stereoselective 1,4-conjugate additions to a D-glucose-derived cyclohex-2-enone derivative, see
    • For highly stereoselective 1,4-conjugate additions to a D-glucose-derived cyclohex-2-enone derivative, see: Murata, T.; Yanagisawa, Y.; Aoyama, M.; Tsushima, H.; Totani, K.; Ohba, S.; Tadano, K. Tetrahedron: Asymmetry 1998, 9, 4203-4217.
    • (1998) Tetrahedron: Asymmetry , vol.9 , pp. 4203-4217
    • Murata, T.1    Yanagisawa, Y.2    Aoyama, M.3    Tsushima, H.4    Totani, K.5    Ohba, S.6    Tadano, K.7
  • 12
    • 0001741843 scopus 로고    scopus 로고
    • House, H. O.; Wilkins, J. M. J. Org. Chem. 1978, 43, 2443-2454. Also see: Handbook of Reagents for Organic Synthesis: Reagents, Auxiliaries and Catalysis for C-C Bonds; Coates, R. M.; Denmark, S. E., Eds.; Wiley: New York, 1999; pp. 453-457.
    • (1978) J. Org. Chem. , vol.43 , pp. 2443-2454
    • House, H.O.1    Wilkins, J.M.2
  • 19
    • 0038952079 scopus 로고
    • For some reports on the effect of TMSCl in altering the stereochemical outcomes of the conjugate additions, see:(a)
    • For some reports on the effect of TMSCl in altering the stereochemical outcomes of the conjugate additions, see: (a) Goodwin, T. E.; Rothman, N. M.; Salazar, K. L.; Sorrels, S. L. J. Org. Chem. 1992, 57, 2469-2471.
    • (1992) J. Org. Chem. , vol.57 , pp. 2469-2471
    • Goodwin, T.E.1    Rothman, N.M.2    Salazar, K.L.3    Sorrels, S.L.4
  • 20
    • 0026017676 scopus 로고
    • (b) and references cited therein
    • (b) Zhao, S.-K.; Helquist, P. Tetrahedron Lett. 1991, 32, 447-448, and references cited therein.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 447-448
    • Zhao, S.-K.1    Helquist, P.2
  • 23
    • 21144477626 scopus 로고
    • For previous papers on the Claisen rearrangement of the carbohydrate-derived allylic alcohols investigated in our laboratory, see: (a)
    • For previous papers on the Claisen rearrangement of the carbohydrate-derived allylic alcohols investigated in our laboratory, see: (a) Tadano, K.; Isshiki, Y.; Kumagai, T.; Ogawa, S. J. Carbohydr. Chem. 1993, 12, 1-11.
    • (1993) J. Carbohydr. Chem. , vol.12 , pp. 1-11
    • Tadano, K.1    Isshiki, Y.2    Kumagai, T.3    Ogawa, S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.