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Volumn 73, Issue 19, 2008, Pages 7710-7720

Intramolecular 1,8-hydrogen atom transfer. Stereoselectivity of the hexopyranos-5′-yl radical reactions in Hexp-(1→4)-Hexp disaccharide systems

Author keywords

[No Author keywords available]

Indexed keywords

ATOMIC PHYSICS; ATOMS; CHEMICAL REACTIONS; HYDROGEN; NONMETALS; POLYSACCHARIDES; REACTION KINETICS; STEREOSELECTIVITY;

EID: 53049100233     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo801499d     Document Type: Article
Times cited : (18)

References (51)
  • 1
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    • Renaud, P, Sibi, M. P, Eds, Wiley-VCH: Weinheim
    • (a) Renaud, P. In Radicals in Organic Synthesis; Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim, 2001; Vol. 1, pp 400-415.
    • (2001) Radicals in Organic Synthesis , vol.1 , pp. 400-415
    • Renaud, P.1
  • 11
    • 0000093228 scopus 로고    scopus 로고
    • For a recent review on radicals in carbohydrate chemistry, see: a, Renaud, P, Sibi, M. P, Eds, Wiley-VCH: Weinheim
    • For a recent review on radicals in carbohydrate chemistry, see: (a) Pearce, A. J.; Mallet, J.-M.; Sinaÿ, P. In Radicals in Organic Synthesis; Renaud, P.; Sibi, M. P., Eds.; Wiley-VCH: Weinheim, 2001; Vol. 2, pp 538-577.
    • (2001) Radicals in Organic Synthesis , vol.2 , pp. 538-577
    • Pearce, A.J.1    Mallet, J.-M.2    Sinaÿ, P.3
  • 16
    • 84969300917 scopus 로고    scopus 로고
    • For a review on the preparation of L-iduronic synthons, see: (a) Pellissier, H. Org. Prep. Proced. Int. 2002, 34, 441-465.
    • For a review on the preparation of L-iduronic synthons, see: (a) Pellissier, H. Org. Prep. Proced. Int. 2002, 34, 441-465.
  • 31
    • 53049101527 scopus 로고    scopus 로고
    • This disaccharide model is closely related to α-L-Idop, 1→4-α-D-Glcp, a repetitive unit in heparin glycosaminoglycan
    • This disaccharide model is closely related to α-L-Idop- (1→4)-α-D-Glcp, a repetitive unit in heparin glycosaminoglycan.
  • 41
    • 0004288915 scopus 로고    scopus 로고
    • For a review on disaccharide synthesis with trichloroacetimidates, see: c, Hanessian, S, Ed, Marcel Dekker: New York
    • For a review on disaccharide synthesis with trichloroacetimidates, see: (c) Schmidt, R. R.; Jung, K.-H. In Preparative Carbohydrate Chemistry; Hanessian, S., Ed.; Marcel Dekker: New York, 1997; pp 283-312.
    • (1997) Preparative Carbohydrate Chemistry , pp. 283-312
    • Schmidt, R.R.1    Jung, K.-H.2
  • 44
    • 53049083262 scopus 로고    scopus 로고
    • eq).
    • eq).
  • 45
    • 0001271574 scopus 로고    scopus 로고
    • For a review, see: a, Renaud, P, Sibi, M. P, Eds, Wiley-VCH: Weinheim
    • For a review, see: (a) Crich, D. In Radicals in Organic Synthesis; Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim, 2001; Vol. 2, pp 188-206.
    • (2001) Radicals in Organic Synthesis , vol.2 , pp. 188-206
    • Crich, D.1
  • 46
    • 0034723342 scopus 로고    scopus 로고
    • For a related 1,5-HAT-intramolecular cine substitution reaction, see: (b) Crich, D.; Huang, X.; Newcomb, M. J. Org. Chem. 2000, 65, 523-529.
    • For a related 1,5-HAT-intramolecular cine substitution reaction, see: (b) Crich, D.; Huang, X.; Newcomb, M. J. Org. Chem. 2000, 65, 523-529.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.