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Volumn 63, Issue 15, 1998, Pages 5137-5143

Ligand Recognition by E- and P-Selectin: Chemoenzymatic Synthesis and Inhibitory Activity of Bivalent Sialyl Lewis x Derivatives and Sialyl Lewis x Carboxylic Acids

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EID: 0001548741     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo980350s     Document Type: Article
Times cited : (46)

References (65)
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    • 1H NMR). Their formation is probably due to the presence of excess of base leading to further alkylation of the acidic α-position of the α-oxy-substituted esters present in the products. (A low-yield alkylation of 5 is also reported in: Jaeger, D. A.; Whitney, R. R. J. Org. Chem. 1975, 40, 92-97.) The overalkylation is not observed under the reaction conditions described here (reverse addition and PTC, respectively).
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 3394-3396
    • Royer, G.P.1    Anantharmaiah, G.M.2
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    • 0000841304 scopus 로고
    • 1H NMR). Their formation is probably due to the presence of excess of base leading to further alkylation of the acidic α-position of the α-oxy-substituted esters present in the products. (A low-yield alkylation of 5 is also reported in: Jaeger, D. A.; Whitney, R. R. J. Org. Chem. 1975, 40, 92-97.) The overalkylation is not observed under the reaction conditions described here (reverse addition and PTC, respectively).
    • (1981) Makromol. Chem. , vol.182 , pp. 1379-1384
    • Brückmann, A.F.1    Morr, M.2
  • 61
    • 0027597847 scopus 로고
    • 1H NMR). Their formation is probably due to the presence of excess of base leading to further alkylation of the acidic α-position of the α-oxy-substituted esters present in the products. (A low-yield alkylation of 5 is also reported in: Jaeger, D. A.; Whitney, R. R. J. Org. Chem. 1975, 40, 92-97.) The overalkylation is not observed under the reaction conditions described here (reverse addition and PTC, respectively).
    • (1993) Pept. Res. , vol.6 , pp. 140-146
    • Lu, Y.-A.1    Felix, A.M.2
  • 62
    • 33847802514 scopus 로고
    • 1H NMR). Their formation is probably due to the presence of excess of base leading to further alkylation of the acidic α-position of the α-oxy-substituted esters present in the products. (A low-yield alkylation of 5 is also reported in: Jaeger, D. A.; Whitney, R. R. J. Org. Chem. 1975, 40, 92-97.) The overalkylation is not observed under the reaction conditions described here (reverse addition and PTC, respectively).
    • (1975) J. Org. Chem. , vol.40 , pp. 92-97
    • Jaeger, D.A.1    Whitney, R.R.2
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    • note
    • 7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.