메뉴 건너뛰기




Volumn 45, Issue 10, 2004, Pages 2171-2175

Development of a novel ionic support and its application in the ionic liquid phase assisted synthesis of a potent antithrombotic

Author keywords

Ionic liquid; Multistep synthesis; Sulfonamide; Supported chemistry; Tirofiban

Indexed keywords

AMIDE; ANTICOAGULANT AGENT; IMIDAZOLE DERIVATIVE; SULFONAMIDE; TIROFIBAN;

EID: 1242317869     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.01.032     Document Type: Article
Times cited : (56)

References (49)
  • 2
    • 0004041607 scopus 로고    scopus 로고
    • G. Jung. Weinheim: Wiley-VCH
    • Jung G. Combinatorial Chemistry. 1999;Wiley-VCH, Weinheim.
    • (1999) Combinatorial Chemistry
  • 20
    • 0004145285 scopus 로고    scopus 로고
    • P. Wasserscheid, & T. Welton. Weinheim: Wiley-VCH
    • Wasserscheid P., Welton T. Ionic Liquids in Synthesis. 2003;Wiley-VCH, Weinheim.
    • (2003) Ionic Liquids in Synthesis
  • 28
    • 0004145285 scopus 로고    scopus 로고
    • Task-specific ionic liquids: P. Wasserscheid, & T. Welton. Weinheim: Wiley-VCH
    • Task-specific ionic liquids: Wasserscheid P., Welton T. Ionic Liquids in Synthesis. 2003;33-40 Wiley-VCH, Weinheim.
    • (2003) Ionic Liquids in Synthesis , pp. 33-40
  • 41
    • 85030893873 scopus 로고    scopus 로고
    • note
    • 2O, respectively).
  • 42
    • 85030903346 scopus 로고    scopus 로고
    • note
    • 2.
  • 43
    • 85030912354 scopus 로고    scopus 로고
    • note
    • 3, 400 MHz), 9a : δ 2.43 (s, 3H), 2.70 (t, 2H), 3.18 (q, 2H), 3.79 (s, 3H), 4.27 (t, 1H), 6.81 (d, 2H), 6.99 (d, 2H), 7.29 (d, 2H), 7.70 (d, 2H); 9b : δ 2.43 (s, 3H), 2.71 (t, 2H), 3.19 (q, 2H), 3.82 (s, 3H), 3.84 (s, 3H), 4.27 (t, 1H), 6.56 (d, 1H), 6.63 (dd, 1H), 6. 77 (d, 1H), 7.28 (d, 2H), 7.67 (d, 2H); 9c : δ 1.06-1.27 (m, 5H), 1.47-1.78 (m, 6H), 2.43 (s, 3H), 3.12 (q, 2H), 4.32 (d, 1H), 7.30 (d, 2H), 7.76 (d, 2H); 9d : δ 2.38 (s, 3H), 3.87 (s, 3H), 4.20 (t, 1H), 7.11 (d, 2H), 7.34 (d, 2H), 7.72 (d, 2H), 7.92 (d, 2H); 10a : δ 2.38 (s, 3H), 2.87 (t, 2H), 3.67 (q, 2H), 3.81 (s, 3H), 6.06 (b, 1H), 6.87 (d, 2H), 7.15 (d, 2H), 7.21 (d, 2H), 7.59 (d, 2H); 10b : δ 2.39 (s, 3H), 2.88 (t, 2H), 3.69 (q, 2H), 3.84 (s, 3H), 3.88 (s, 3H), 6.74-6.84 (m, 3H), 7.21 (d, 2H), 7.59 (d, 2H); 10c : δ 1.16-1.29 (m, 3H), 1.38-1.49 (m, 2H), 1.62-1.70 (m, 1H), 1.72-1.79 (m, 2H), 1.99-2.08 (m, 2H), 2.39 (s, 3H), 3.92-4.02 (m, 1H), 6.11 (bs, 1H), 7.22 (d, 2H), 7.64 (d, 2H); 10d : δ 2.44 (s, 3H), 3.92 (s, 3H), 7.31 (d, 2H), 7. 74 (d, 2H), 7.78 (d, 2H), 8.06 (d, 2H).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.