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Volumn 14, Issue 5, 2004, Pages 1129-1132

Carbazolothiophene-2-carboxylic acid derivatives as endothelin receptor antagonists

Author keywords

Coupling reactions; Endothelin; Indole; Samarium diiodide; Thiophene

Indexed keywords

3 (2 CARBOXYMETHOXY 4 METHOXYPHENYL) 1 (3,4 METHYLENEDIOXYPHENYL) 5 PROPOXY 2 INDANCARBOXYLIC ACID; 9 BENZYL 4 METHYL 4 (4 HYDROXYPHENYL) 10 OXO 4,10 DIHYDROCARBAZOLO[2,3 B]THIOPHENE 2 CARBOXYLIC ACID; ACETOPHENONE; CALCIUM ION; CARBAZOLE DERIVATIVE; CARBAZOLOTHIOPHENE 2 CARBOXYLIC ACID DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; CYCLO(DEXTRO TRYPTOPHYL DEXTRO ASPARTYLPROLYL DEXTRO VALYLLEUCYL); ENDOTHELIN 1; ENDOTHELIN RECEPTOR ANTAGONIST; INDOLE 2 CARBALDEHYDE; INDOLE DERIVATIVE; PD 159433; SAMARIUM DIIODIDE; SB 209598; SITAXSENTAN; THIOPHENE 2 CARBOXYLATE; THIOPHENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 1242271969     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2003.12.067     Document Type: Article
Times cited : (11)

References (27)
  • 10
    • 85030896586 scopus 로고    scopus 로고
    • PCT Int. Appl. 1994, 48 pp WO 9414434 A1 19940707
    • Elliott, J. D.; Leber, J. D. PCT Int. Appl. 1994, 48 pp WO 9414434 A1 19940707.
    • Elliott, J.D.1    Leber, J.D.2
  • 18
    • 85030898861 scopus 로고    scopus 로고
    • note
    • 3) δ 7.61 (s, 1H), 7.58 (dd, 1H, J=8.4, 1.2 Hz), 7.35-7.18 (m, 9H), 7.02 (dt, 1H, J=7.6, 0.8 Hz), 6.78 (td, 2H, J=8.8, 3.2 Hz), 6.16 (d, 1H, J=16.0 Hz), 6. 11 (d, 1H, J=16.0 Hz), 2.19 (s, 3H). 19: mp 244-245°C. 20: mp 217-218°C. 21: mp 291-292°C. 22: mp 150-151°C.
  • 19
    • 0001938996 scopus 로고
    • For use of hexamethylphosphoramide (HMPA) as a general additive to samarium diiodide in reaction acceleration and regiochemical control, see:
    • For use of hexamethylphosphoramide (HMPA) as a general additive to samarium diiodide in reaction acceleration and regiochemical control, see: Inanaga J., Ishikawa M., Yamaguchi H. Chem. Lett. 1987;1485.
    • (1987) Chem. Lett. , pp. 1485
    • Inanaga, J.1    Ishikawa, M.2    Yamaguchi, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.