메뉴 건너뛰기




Volumn 67, Issue 29, 2011, Pages 5142-5149

A facile synthesis of indole-furan conjugates via integration of convergent and linear domino reactions

Author keywords

Biheteroaryls; Domino reaction; Friedel Crafts alkylation; Furan; Indole; Paal Knorr cyclization

Indexed keywords

1 [4 (1H INDOL 3 YL) 2 METHYL 5 PHENYLFURAN 3 YL]ETHANONE; 3 [2,5 BIS(4 METHOXYPHENYL) 4 (METHYLTHIO)FURAN 3 YL] 1H INDOLE; 3 [4 (METHYLTHIO) 2,5 BIS(4 NITROPHENYL)FURAN 3 YL] 1H INDOLE; 3 [4 (METHYLTHIO) 2,5 BIS(4 TOLYLFURAN) 3 YL] 1H INDOLE; 3 [4 (METHYLTHIO) 2,5 BIS(NAPHTHALEN 2 YL)FURAN 3 YL] 1H INDOLE; 3 [4 (METHYLTHIO) 2,5 DIPHENYLFURAN 3 YL] 1H INDOLE; [4 (1H INDOL 3 YL) 2,5 DIPHENYLFURAN 3 YL](PHENYL)METHANONE; ETHYL 4 (1 METHYL 1H INDOL 3 YL) 2,5 DIPHENYLFURAN 3 CARBOXYLIC ACID; ETHYL 4 (1H INDOL 3 YL) 2 (3 NITROPHENYL) 5 PHENYLFURAN 3 CARBOXYLIC ACID; ETHYL 4 (1H INDOL 3 YL) 2 PHENYL 5 (4 TOLYLFURAN) 3 CARBOXYLIC ACID; ETHYL 4 (1H INDOL 3 YL) 2 PHENYL 5 (THIOPHEN 3 YL)FURAN 3 CARBOXYLIC ACID; ETHYL 4 (1H INDOL 3 YL) 2,5 DIPHENYLFURAN 3 CARBOXYLIC ACID; ETHYL 4 (1H INDOL 3 YL) 5 (4 METHOXYPHENYL) 2 PHENYLFURAN 3 CARBOXYLIC ACID; ETHYL 4 (1H INDOL 3 YL) 5 (4 NITROPHENYL) 2 PHENYLFURAN 3 CARBOXYLIC ACID; ETHYL 4 (1H INDOL 3 YL) 5 (NAPHTHALEN 1 YL) 2 PHENYLFURAN 3 CARBOXYLIC ACID; ETHYL 4 (1H INDOL 3 YL) 5 (NAPHTHALEN 2 YL) 2 PHENYLFURAN 3 CARBOXYLIC ACID; ETHYL 4 (1H INDOL 3 YL) 5 PHENYL 2 (3,4,5 TRIMETHOXYPHENYL)FURAN 3 CARBOXYLIC ACID; ETHYL 4 (1H INDOL 3 YL) 5 PHENYL 2,2' BIFURAN 3 CARBOXYLIC ACID; ETHYL 5 (3,4 DICHLOROPHENYL) 4 (1H INDOL 3 YL) 2 PHENYLFURAN 3 CARBOXYLIC ACID; ETHYL 5 (4 BROMOPHENYL) 4 (1H INDOL 3 YL) 2 PHENYLFURAN 3 CARBOXYLIC ACID; ETHYL 5 (4 CHLOROPHENYL) 4 (1H INDOL 3 YL) 2 PHENYLFURAN 3 CARBOXYLIC ACID; ETHYL 5 (4 FLUOROPHENYL) 4 (1H INDOL 3 YL) 2 PHENYLFURAN 3 CARBOXYLIC ACID; ETHYL 5 (4 HYDROXYPHENYL) 4 (1H INDOL 3 YL) 2 PHENYLFURAN 3 CARBOXYLIC ACID; ETHYL 5 (BENZOFURAN 2 YL) 4 (1H INDOL 3 YL) 2 PHENYLFURAN 3 CARBOXYLIC ACID; FURAN DERIVATIVE; INDOLE DERIVATIVE; KETONE; METHYL 2 (4 CHLOROPHENYL) 4 (1H INDOL 3 YL) 5 PHENYLFURAN 3 CARBOXYLIC ACID; METHYL 2 (4 FLUOROPHENYL) 4 (1H INDOL 3 YL) 5 PHENYLFURAN 3 CARBOXYLIC ACID; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 79958770155     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.05.058     Document Type: Article
Times cited : (41)

References (41)
  • 11
  • 15
    • 85016884664 scopus 로고    scopus 로고
    • For reviews, see: (a)
    • For reviews, see: (a) Steel, P. J. Adv. Heterocycl. Chem. 1996, 67, 1-117;
    • (1996) Adv. Heterocycl. Chem. , vol.67 , pp. 1-117
    • Steel, P.J.1
  • 23
    • 79958773178 scopus 로고    scopus 로고
    • PCT Int. Appl. WO US 2006/0122232 A1
    • (c) Chou, S. Y.; Chen, S. S. T.; Tsai, H. J. PCT Int. Appl. WO US 2006/0122232 A1, 2006.
    • (2006)
    • Chou, S.Y.1    Chen, S.S.T.2    Tsai, H.J.3
  • 25
    • 79958765465 scopus 로고    scopus 로고
    • note
    • The 1,4-enediones 2 and 3 were used as a mixture of isomers. Due to the reaction mechanism, they lead solely to the 3-furyl-substituted indoles.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.