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Volumn 40, Issue 9, 2001, Pages 1670-1673

Synthesis of conformationally locked carbohydrates: A skew-boat conformation of L-iduronic acid governs the antithrombotic activity of heparin

Author keywords

Blood coagulation; Carbohydrates; Glycosylation; Heparin; Molecular recognition

Indexed keywords

BLOOD; COAGULATION; CONFORMATIONS; SYNTHESIS (CHEMICAL);

EID: 0035805327     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3773(20010504)40:9<1670::AID-ANIE16700>3.0.CO;2-Q     Document Type: Article
Times cited : (66)

References (29)
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    • 0342426452 scopus 로고    scopus 로고
    • note
    • A full account of the syntheses of 3 and 4 will be separately described elsewhere.
  • 21
    • 0342426453 scopus 로고    scopus 로고
    • note
    • In the case of the pentasaccharide 4, the glucuronic acid unit E has also heen modified, with the H-5 atom being replaced by an ethyl group. This is a direct consequence of the selected converging strategy that has been selected for the sake of simplicity. We have, however, shown that replacement of the H-5 atom by an ethyl group in compound 1 does not affect its biological activity (see Table 1).
  • 24


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.