메뉴 건너뛰기




Volumn 44, Issue 8, 2005, Pages 1210-1212

Direct organocatalytic de novo synthesis of carbohydrates

Author keywords

Aldol reaction; Amino sugars; Asymmetric synthesis; Carbohydrates; Organocatalysis

Indexed keywords

ALCOHOLS; ALDEHYDES; AMINO ACIDS; CATALYSIS; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 15444380834     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200462428     Document Type: Article
Times cited : (221)

References (49)
  • 2
    • 0035805264 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2001, 40, 1576-1624;
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 1576-1624
  • 3
    • 15444371447 scopus 로고    scopus 로고
    • (Ed.: Y. Chapleur), Wiley-VCH, Weinheim
    • b) Carbohydrats Mimics (Ed.: Y. Chapleur), Wiley-VCH, Weinheim, 1998.
    • (1998) Carbohydrats Mimics
  • 4
    • 0004285044 scopus 로고    scopus 로고
    • (Ed.: S. M. Hecht), Oxford University Press, New York
    • a) M. Sznaidman in Bioorganic Chemistry: Carbohydrates (Ed.: S. M. Hecht), Oxford University Press, New York, 1999, pp. 1-56;
    • (1999) Bioorganic Chemistry: Carbohydrates , pp. 1-56
    • Sznaidman, M.1
  • 8
    • 0000492601 scopus 로고
    • H. Kunz, K. Rück, Angew. Chem. 1993, 105, 355-377; Angew. Chem. Int. Ed. Engl. 1993, 32, 336-358.
    • (1993) Angew. Chem. , vol.105 , pp. 355-377
    • Kunz, H.1    Rück, K.2
  • 9
    • 33748831238 scopus 로고
    • H. Kunz, K. Rück, Angew. Chem. 1993, 105, 355-377; Angew. Chem. Int. Ed. Engl. 1993, 32, 336-358.
    • (1993) Angew. Chem. Int. Ed. Engl. , vol.32 , pp. 336-358
  • 12
    • 0029739240 scopus 로고    scopus 로고
    • b) S. J. Danishefsky, M. T. Bilodeau, Angew. Chem. 1996, 108, 1482-1522; Angew. Chem. Int. Ed. Engl. 1996, 35, 1380-1520;
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 1380-1520
  • 16
    • 3242806955 scopus 로고    scopus 로고
    • a) A. B. Northrup, I. K. Mangion, F. Hettche, D. W. C. MacMillan, Angew. Chem. 2004, 116, 2004-2006; Angew. Chem. Int. Ed. 2004, 43, 2152-2154;
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 2152-2154
  • 18
    • 0008286974 scopus 로고
    • M. Calvin, Angew. Chem. 1962, 74, 165-175; Angew. Chem. Int. Ed. Engl. 1962, 1, 65-75.
    • (1962) Angew. Chem. , vol.74 , pp. 165-175
    • Calvin, M.1
  • 19
    • 85027475990 scopus 로고
    • M. Calvin, Angew. Chem. 1962, 74, 165-175; Angew. Chem. Int. Ed. Engl. 1962, 1, 65-75.
    • (1962) Angew. Chem. Int. Ed. Engl. , vol.1 , pp. 65-75
  • 20
    • 15444362586 scopus 로고    scopus 로고
    • Enolates, organocatalysis, biocatalysis and natural Product synthesis
    • W.-D. Fessner (Ed.: R. Mahrwald), Wiley-VCH, Weinheim
    • a) "Enolates, Organocatalysis, Biocatalysis and Natural Product Synthesis": W.-D. Fessner in Modern Aldol Reactions, Vol. 1 (Ed.: R. Mahrwald), Wiley-VCH, Weinheim, 2004, 201-272;
    • (2004) Modern Aldol Reactions , vol.1 , pp. 201-272
  • 22
    • 0034678591 scopus 로고    scopus 로고
    • b) C.-H. Wong, T. D. Machajewski, Angew. Chem. 2000, 112, 1206-1230; Angew. Chem. Int. Ed. 2000, 39, 1352-1375;
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 1352-1375
  • 27
    • 15444367146 scopus 로고    scopus 로고
    • in press
    • Review: D. Enders, M. Voith, A. Lenzen, Angew. Chem. 2005, 117; Angew. Chem. Int. Ed. 2005, 44, in press.
    • (2005) Angew. Chem. Int. Ed. , vol.44
  • 29
    • 0034596299 scopus 로고    scopus 로고
    • b) For an efficient proline-catalyzed aldol reaction of hydroxy acetone with aldehydes see: W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386-7387.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 7386-7387
    • Notz, W.1    List, B.2
  • 30
    • 0036996359 scopus 로고    scopus 로고
    • Dioxanone 1 can be synthesized easily by undergraduate students on a 1-mol scale from simple precursors and is also commercially available, a) D. Enders, M. Voith, S. J. Ince, Synthesis 2002, 1775-1779;
    • (2002) Synthesis , pp. 1775-1779
    • Enders, D.1    Voith, M.2    Ince, S.J.3
  • 33
    • 15444364155 scopus 로고    scopus 로고
    • note
    • Freshly prepared 2e was used for the aldol reaction due to its tendency for polymerization and racemization.
  • 37
    • 13644256524 scopus 로고    scopus 로고
    • Enolates, organocatalysis, biocatalysis and natural product synthesis
    • (Ed.: R. Mahrwald), Wiley-VCH, Weinheim
    • "Enolates, Organocatalysis, Biocatalysis and Natural Product Synthesis": B. List in Modern Aldol Reactions, Vol. 1 (Ed.: R. Mahrwald), Wiley-VCH, Weinheim, 2004, 161-200.
    • (2004) Modern Aldol Reactions , vol.1 , pp. 161-200
    • List, B.1
  • 46
    • 0001811560 scopus 로고
    • a) W.-D. Fessner, O. Eyrisch, Angew. Chem. 1992, 104, 76-78; Angew. Chem. Int. Ed. Engl. 1992, 31, 56-58;
    • (1992) Angew. Chem. Int. Ed. Engl. , vol.31 , pp. 56-58


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.