메뉴 건너뛰기




Volumn 1-4, Issue , 2007, Pages 489-582

Synthesis of Monosaccharides and Analogs

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84876295420     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1016/B978-044451967-2/00014-3     Document Type: Chapter
Times cited : (6)

References (516)
  • 9
    • 1642407159 scopus 로고    scopus 로고
    • Springer, Berlin, Germany, Chapter 4.4, B. Fraser-Reid, K. Tatsuta, J. Thiem (Eds.)
    • Vogel P. Encyclopedia of Glycosciences 2001, Vol. 2:1023-1174. Springer, Berlin, Germany, Chapter 4.4. B. Fraser-Reid, K. Tatsuta, J. Thiem (Eds.).
    • (2001) Encyclopedia of Glycosciences , vol.2 , pp. 1023-1174
    • Vogel, P.1
  • 10
    • 33645788031 scopus 로고    scopus 로고
    • CRC Taylor & Francis Group, Boca Raton, FL, Chapter 13, D.E. Levy, P. Fügedi (Eds.)
    • Vogel P. The Organic Chemistry of Sugars 2006, 629-725. CRC Taylor & Francis Group, Boca Raton, FL, Chapter 13. D.E. Levy, P. Fügedi (Eds.).
    • (2006) The Organic Chemistry of Sugars , pp. 629-725
    • Vogel, P.1
  • 19
    • 34548274697 scopus 로고
    • Decker P. Umschau 1973, 73:733-734.
    • (1973) Umschau , vol.73 , pp. 733-734
    • Decker, P.1
  • 59
  • 92
    • 0001370275 scopus 로고
    • For reviews, see, for example
    • Cohen N. Acc. Chem. Res. 1976, 9:412-417. For reviews, see, for example.
    • (1976) Acc. Chem. Res. , vol.9 , pp. 412-417
    • Cohen, N.1
  • 93
    • 0037043180 scopus 로고    scopus 로고
    • List B. Tetrahedron 2002, 58:5573-5590.
    • (2002) Tetrahedron , vol.58 , pp. 5573-5590
    • List, B.1
  • 98
    • 0034750244 scopus 로고    scopus 로고
    • List B. Synlett 2001, 1675-1686.
    • (2001) Synlett , pp. 1675-1686
    • List, B.1
  • 111
    • 23444453354 scopus 로고    scopus 로고
    • For 4-substituted prolines
    • Bellis E., Kokotos G. Tetrahedon 2005, 61:8669-8676. For 4-substituted prolines.
    • (2005) Tetrahedon , vol.61 , pp. 8669-8676
    • Bellis, E.1    Kokotos, G.2
  • 112
    • 0037037912 scopus 로고    scopus 로고
    • For protonic acid - cyclic and acyclic 2-aminomethyl pirrolidines
    • Nakada M., Saito S., Yamamoto H. Tetrahedron 2002, 58:8167-8177. For protonic acid - cyclic and acyclic 2-aminomethyl pirrolidines.
    • (2002) Tetrahedron , vol.58 , pp. 8167-8177
    • Nakada, M.1    Saito, S.2    Yamamoto, H.3
  • 166
    • 0003129117 scopus 로고
    • Otto Salle Verlag, Verlag Sauerländer, Frankfurt, Germany, R. Scheffold (Ed.)
    • Seebach D., Hungerbühler E. Modern Synthetic Methods 1980, Vol. 2:91-171. Otto Salle Verlag, Verlag Sauerländer, Frankfurt, Germany. R. Scheffold (Ed.).
    • (1980) Modern Synthetic Methods , vol.2 , pp. 91-171
    • Seebach, D.1    Hungerbühler, E.2
  • 214
    • 79952603224 scopus 로고
    • American Chemical Society, Washington, DC, Chapter 15, D. Horton, L.D. Hawkins, G.D. McGarvey (Eds.)
    • Mukaiyama T. Trends in Synthetic Carbohydrate Chemistry, ACS Symposium Series 386 1989, 278-289. American Chemical Society, Washington, DC, Chapter 15. D. Horton, L.D. Hawkins, G.D. McGarvey (Eds.).
    • (1989) Trends in Synthetic Carbohydrate Chemistry, ACS Symposium Series 386 , pp. 278-289
    • Mukaiyama, T.1
  • 219
    • 0037454978 scopus 로고    scopus 로고
    • For other nucleophilic additions to sugar-derived aldehydes, see
    • Ulgheri F., Bacsa J., Nassimbeni L., Spanu P. Tetrahedron Lett. 2003, 44:671-675. For other nucleophilic additions to sugar-derived aldehydes, see.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 671-675
    • Ulgheri, F.1    Bacsa, J.2    Nassimbeni, L.3    Spanu, P.4
  • 246
    • 29344454053 scopus 로고    scopus 로고
    • For an alternative approach, see
    • Fürstner A., Wuchrer M. Chem. Eur. J. 2006, 12:76-89. For an alternative approach, see.
    • (2006) Chem. Eur. J. , vol.12 , pp. 76-89
    • Fürstner, A.1    Wuchrer, M.2
  • 272
    • 0034714493 scopus 로고    scopus 로고
    • For other three-carbon homologations, see, for example
    • Majewski M., Nowak P. J. Org. Chem. 2000, 65:5152-5160. For other three-carbon homologations, see, for example.
    • (2000) J. Org. Chem. , vol.65 , pp. 5152-5160
    • Majewski, M.1    Nowak, P.2
  • 305
    • 33544463124 scopus 로고    scopus 로고
    • For other examples of hetero-Diels-Alder additions of aldehydes, see
    • Osborn H.M.I., Coisson D. Mini-Rev. Org. Chem. 2004, 1:41-54. For other examples of hetero-Diels-Alder additions of aldehydes, see.
    • (2004) Mini-Rev. Org. Chem. , vol.1 , pp. 41-54
    • Osborn, H.M.I.1    Coisson, D.2
  • 377
    • 0033607764 scopus 로고    scopus 로고
    • For other enantiomerically enriched 7-oxabicyclo[2.2.1]heptane derivatives, see
    • Vogel P., Cossy J., Plumet J., Arjona O. Tetrahedron 1999, 55:13521-13642. For other enantiomerically enriched 7-oxabicyclo[2.2.1]heptane derivatives, see.
    • (1999) Tetrahedron , vol.55 , pp. 13521-13642
    • Vogel, P.1    Cossy, J.2    Plumet, J.3    Arjona, O.4
  • 489
    • 0029988590 scopus 로고    scopus 로고
    • For other applications, see
    • Xu Y.-M., Zhou W.-S. Tetrahedron Lett. 1996, 37:1461-1462. For other applications, see.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 1461-1462
    • Xu, Y.-M.1    Zhou, W.-S.2
  • 513
    • 0033538110 scopus 로고    scopus 로고
    • For further applications of asymmetric dihydroxylation, for example
    • Lemaire-Audoire S., Vogel P. Tetrahedron: Asymmetry 1999, 10:1283-1293. For further applications of asymmetric dihydroxylation, for example.
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 1283-1293
    • Lemaire-Audoire, S.1    Vogel, P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.