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Volumn 9, Issue 22, 1998, Pages 3939-3943

Branched-chain functionalised carbohydrates via β-functionalised organolithium compounds

Author keywords

[No Author keywords available]

Indexed keywords

CARBOHYDRATE DERIVATIVE; EPOXIDE; ORGANOLITHIUM COMPOUND; WATER;

EID: 0032573614     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(98)00411-X     Document Type: Article
Times cited : (32)

References (32)
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    • See, for instance: Borman S. Chem. Eng. News 1998, 76, July 20, 49.
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    • Borman, S.1
  • 2
    • 0003433653 scopus 로고
    • Pergamon Press: Oxford
    • See, for instance: (a) Hanessian, S. Total Synthesis of Natural Products: The Chiron Approach; Pergamon Press: Oxford, 1983. (b) Lichtenthaler, F. In Modern Synthetic Methods 1992; Scheffold, R., Ed.; VCA Publishers: New York, 1992; p. 273. (c) Bols, M. Carbohydrate Building Blocks; John Wiley & Sons: New York, 1996.
    • (1983) Total Synthesis of Natural Products: The Chiron Approach
    • Hanessian, S.1
  • 3
    • 0003087447 scopus 로고
    • Scheffold, R., Ed.; VCA Publishers: New York
    • See, for instance: (a) Hanessian, S. Total Synthesis of Natural Products: The Chiron Approach; Pergamon Press: Oxford, 1983. (b) Lichtenthaler, F. In Modern Synthetic Methods 1992; Scheffold, R., Ed.; VCA Publishers: New York, 1992; p. 273. (c) Bols, M. Carbohydrate Building Blocks; John Wiley & Sons: New York, 1996.
    • (1992) Modern Synthetic Methods 1992 , pp. 273
    • Lichtenthaler, F.1
  • 4
    • 0004285331 scopus 로고    scopus 로고
    • John Wiley & Sons: New York
    • See, for instance: (a) Hanessian, S. Total Synthesis of Natural Products: The Chiron Approach; Pergamon Press: Oxford, 1983. (b) Lichtenthaler, F. In Modern Synthetic Methods 1992; Scheffold, R., Ed.; VCA Publishers: New York, 1992; p. 273. (c) Bols, M. Carbohydrate Building Blocks; John Wiley & Sons: New York, 1996.
    • (1996) Carbohydrate Building Blocks
    • Bols, M.1
  • 7
    • 37049073704 scopus 로고
    • (a) For the first account of this reaction, see: Yus, M.; Ramón, D. J. J. Chem. Soc., Chem. Commun. 1991, 398. (b) For a review, see: Yus, M. Chem. Soc. Rev. 1996, 155.
    • (1991) J. Chem. Soc., Chem. Commun. , pp. 398
    • Yus, M.1    Ramón, D.J.2
  • 8
    • 0030496093 scopus 로고    scopus 로고
    • (a) For the first account of this reaction, see: Yus, M.; Ramón, D. J. J. Chem. Soc., Chem. Commun. 1991, 398. (b) For a review, see: Yus, M. Chem. Soc. Rev. 1996, 155.
    • (1996) Chem. Soc. Rev. , pp. 155
    • Yus, M.1
  • 25
    • 85038541323 scopus 로고    scopus 로고
    • note
    • 2; c 1.08). (equation presented)
  • 26
    • 85038553788 scopus 로고    scopus 로고
    • note
    • o). The enantiomorph was fixed according to the known stereochemistry of four of the chiral centres in the molecule, (b) Data were processed on an AlphaStation 200 4/166 (OpenVMS Alpha V6.2), using the program XCAD4B (K. Harms, University of Marburg) and the commercial package SHELXTL-PLUS Release 5.05/V. © 1996 Siemens Analytical X-Ray Instruments, Inc., Madison, WI. (c) SHELXS-97: Fortran program for crystal structure solution. © 1997 G. M. Sheldrick. (d) SHELXL-97: Fortran program for crystal structure solution. © 1997 G. M. Sheldrick.
  • 27
    • 85038547265 scopus 로고    scopus 로고
    • note
    • 2; c 1.2).
  • 28
    • 85038551228 scopus 로고    scopus 로고
    • note
    • 2; c 1.26).
  • 29
    • 85038541916 scopus 로고    scopus 로고
    • note
    • 2; c 1.10).
  • 30
    • 0000665936 scopus 로고    scopus 로고
    • 15 takes place to the convex β-position by the preferential control due to the rigid bicyclic structure. See, for instance: (a) Peterson, M. A.; Mitchell, J. R. J. Org. Chem. 1997, 62, 8237. (b) Yamauchi, N.; Kishida, M.; Sawada, K.; Ohashi, Y.; Eguchi, T.; Kakinura, K. Chem. Lett. 1998, 475. (c) See also Ref. 4.
    • (1997) J. Org. Chem. , vol.62 , pp. 8237
    • Peterson, M.A.1    Mitchell, J.R.2
  • 31
    • 0032364306 scopus 로고    scopus 로고
    • 15 takes place to the convex β-position by the preferential control due to the rigid bicyclic structure. See, for instance: (a) Peterson, M. A.; Mitchell, J. R. J. Org. Chem. 1997, 62, 8237. (b) Yamauchi, N.; Kishida, M.; Sawada, K.; Ohashi, Y.; Eguchi, T.; Kakinura, K. Chem. Lett. 1998, 475. (c) See also Ref. 4.
    • (1998) Chem. Lett. , pp. 475
    • Yamauchi, N.1    Kishida, M.2    Sawada, K.3    Ohashi, Y.4    Eguchi, T.5    Kakinura, K.6
  • 32
    • 85038540874 scopus 로고    scopus 로고
    • See also Ref. 4
    • 15 takes place to the convex β-position by the preferential control due to the rigid bicyclic structure. See, for instance: (a) Peterson, M. A.; Mitchell, J. R. J. Org. Chem. 1997, 62, 8237. (b) Yamauchi, N.; Kishida, M.; Sawada, K.; Ohashi, Y.; Eguchi, T.; Kakinura, K. Chem. Lett. 1998, 475. (c) See also Ref. 4.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.