메뉴 건너뛰기




Volumn 64, Issue 41, 2008, Pages 9675-9684

Palladium-catalyzed synthesis of quinoxaline derivatives

Author keywords

Palladium catalyzed annulation; Quinoxaline

Indexed keywords

(3,4 DIHYDRO 3,3 DIMETHYLQUINOXALIN 6 YL)PHENYLMETHANONE; 1',4' DIHYDRO 7' METHOXY SPIRO[CYCLOHEXANE 1,2'(3'H)QUINOXALIN]3' ONE; 1,10 PHENANTHROLINE; 1,2 DIHYDRO 2,2 DIMETHYL 7 METHOXYQUINOXALINE; 1,2 DIHYDRO 2,2 DIMETHYLQUINOXALINE; 1,2 DIHYDRO 2,2 DIPHENYL 7 METHOXYQUINOXALINE; 1,2 DIHYDRO 2,2,5 TRIMETHYLQUINOXALINE; 1,2 DIHYDRO 2,2,7 TRIMETHYLQUINOXALINE; 1,2 DIHYDRO 2,2,8 TRIMETHYLQUINOXALINE; 2 PENTYLQUINOXALINE; 2 PENTYLQUINOXALINE 1 OXIDE; 2,2 DIMETHYL 1,2 DIHYDROQUINOXALINE; 3,4 DIHYDRO 3,3 DIMETHYL 2 QUINOXALINONE; 3,4 DIHYDRO 3,3 DIMETHYL 6 METHOXY 2 QUINOXALINONE; 3,4 DIHYDRO 3,3,5 TRIMETHYL 2 QUINOXALINONE; 3,4 DIHYDRO 3,3,8 TRIMETHYL 2 QUINOXALINONE; 6 CHLORO 1,2 DIHYDRO 2,2 DIMETHYLQUINOXALINE; 6 CHLORO 3,4 DIHYDRO 3,3 DIMETHYL 2 QUINOXALINONE; 7 CHLORO 1,2 DIHYDRO 2,2 DIMETHYLQUINOXALINE; 7 CHLORO 2 PHENYLQUINOXALINE; 7 CHLORO 2 PHENYLQUINOXALINE 1 N OXIDE; 7 CHLORO 3,4 DIHYDRO 3,3 DIMETHYL 2 QUINOXALINONE; 7' METHOXY SPIRO[CYCLOHEXANE 1,2'(1'H)QUINOXALINE]; CARBON MONOXIDE; DIHYDRO 3,3,6 TRIMETHYL 2 QUINOXALINONE; ENAMINE; PALLADIUM; QUINOXALINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 49849092121     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.07.083     Document Type: Article
Times cited : (27)

References (59)
  • 1
    • 49849097687 scopus 로고    scopus 로고
    • For reviews, see:
    • For reviews, see:
  • 30
    • 49849095916 scopus 로고    scopus 로고
    • For recent reviews, see:
    • For recent reviews, see:
  • 33
    • 49849096763 scopus 로고    scopus 로고
    • note
    • For a single example of a related selenium-catalyzed reaction under 30 atm of CO forming 2-propylbenzimidazole in 36% yield, see: Ref. 10.
  • 39
    • 49849091051 scopus 로고    scopus 로고
    • note
    • The enamine rapidly decomposes/hydrolyzes and correct analyses could not be obtained.
  • 42
    • 49849099450 scopus 로고    scopus 로고
    • Meichsner, C.; Riess, G.; Kleim, J. P.; Roesner, M.; Paessens, A.; Blunck, M. Eur. Pat. Appl. EP657166, 1995;
    • Meichsner, C.; Riess, G.; Kleim, J. P.; Roesner, M.; Paessens, A.; Blunck, M. Eur. Pat. Appl. EP657166, 1995;
  • 43
    • 49849101087 scopus 로고    scopus 로고
    • Chem. Abstr. 1995, 123, 228218.
    • Chem. Abstr. 1995, 123, 228218.
  • 45
    • 49849096677 scopus 로고    scopus 로고
    • Billhardt, U. M.; Roesner, M.; Riess, G.; Winkler, I.; Bender, R. Eur. Pat. Appl. EP509398, 1992;
    • Billhardt, U. M.; Roesner, M.; Riess, G.; Winkler, I.; Bender, R. Eur. Pat. Appl. EP509398, 1992;
  • 46
    • 49849092939 scopus 로고    scopus 로고
    • Chem. Abstr. 1993, 118, 234088.
    • Chem. Abstr. 1993, 118, 234088.
  • 47
    • 49849085293 scopus 로고    scopus 로고
    • note
    • The compound decomposes and turns dark purple upon standing and a correct elemental analysis could not be obtained.
  • 49
    • 49849094206 scopus 로고    scopus 로고
    • note
    • Although the mp is significantly different form the literature value, the structure of 43 was confirmed by 2D NMR experiments including gHSQC, gHMBC, NOESY, and gCOSY.
  • 51
    • 49849096054 scopus 로고    scopus 로고
    • Suzuki, K.; Komatsu, T.; Ina, S.; Fujii, K.; Kojima, J.; Yamana, K. Jpn. Kokai Tokkyo Koho JP4282314, 1992;
    • Suzuki, K.; Komatsu, T.; Ina, S.; Fujii, K.; Kojima, J.; Yamana, K. Jpn. Kokai Tokkyo Koho JP4282314, 1992;
  • 52
    • 49849091251 scopus 로고    scopus 로고
    • Chem. Abstr. 1993, 118, 73688.
    • Chem. Abstr. 1993, 118, 73688.
  • 53
    • 49849088228 scopus 로고    scopus 로고
    • note
    • Commercially available.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.