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Volumn 78, Issue 1, 2009, Pages 161-168

One-pot synthesis of 1-arylindole-3-carboxylates from 2-(2-isocyanophenyl)acetates

Author keywords

1,1' (1,3 diphenylene)diindole; Benzyl Anion; Flouronitrobenzene; Indole 3 carboxylate; o Tolyl Isocyanide

Indexed keywords


EID: 62549128640     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-08-11509     Document Type: Article
Times cited : (5)

References (23)
  • 4
    • 62549105379 scopus 로고    scopus 로고
    • For recent reports on the biological activity of indole-3-carboxylates
    • For recent reports on the biological activity of indole-3-carboxylates:
  • 7
    • 62549118757 scopus 로고    scopus 로고
    • Indole-3-carboxylates have recently utilized for the synthesis of more complex molecules
    • Indole-3-carboxylates have recently utilized for the synthesis of more complex molecules:
  • 9
    • 62549144481 scopus 로고    scopus 로고
    • For recent syntheses of indole-3-carboxylates
    • For recent syntheses of indole-3-carboxylates:
  • 13
    • 0018385643 scopus 로고
    • Using Nenitzescu reaction;
    • Using Nenitzescu reaction;. Kuckländer U. Arch. Pharm. 312 (1979) 515
    • (1979) Arch. Pharm. , vol.312 , pp. 515
    • Kuckländer, U.1
  • 14
    • 33846120947 scopus 로고    scopus 로고
    • Via PIFA-mediated intramolecular cyclization of 2-aryl-3-arylaminoacrylates:
    • Via PIFA-mediated intramolecular cyclization of 2-aryl-3-arylaminoacrylates:. Du Y., Liu R., Linn G., and Zhao K. Org. Lett. 8 (2006) 5919
    • (2006) Org. Lett. , vol.8 , pp. 5919
    • Du, Y.1    Liu, R.2    Linn, G.3    Zhao, K.4
  • 16
    • 44949150209 scopus 로고    scopus 로고
    • Via a copper-catalyzed reaction of methyl 2-(2-bromophenyl)acetate with methyl formate and arylamines:
    • Via a copper-catalyzed reaction of methyl 2-(2-bromophenyl)acetate with methyl formate and arylamines:. Melkonyan R.S., Karchava A.V., and Yurovskaya A. J. Org. Chem. 73 (2008) 4275
    • (2008) J. Org. Chem. , vol.73 , pp. 4275
    • Melkonyan, R.S.1    Karchava, A.V.2    Yurovskaya, A.3
  • 19
    • 62549107128 scopus 로고    scopus 로고
    • N-4-Nitrophenylation of indole with 4-iodonitrobenzene has been achieved using copper catalysts at higher temperatures 90-160 °C
    • N-4-Nitrophenylation of indole with 4-iodonitrobenzene has been achieved using copper catalysts at higher temperatures (90-160 °C):
  • 22
    • 0038391514 scopus 로고    scopus 로고
    • 1-(2-Nitrophenyl)- and 1-(2,4-dinitrophenyl)indoles have been prepared by N-arylation of indoline-2-carboxylic acid followed by decarboxylation and dehydrogenation;
    • 1-(2-Nitrophenyl)- and 1-(2,4-dinitrophenyl)indoles have been prepared by N-arylation of indoline-2-carboxylic acid followed by decarboxylation and dehydrogenation;. Chicharro R., de Castro S., Reino J.L., and Aran V.J. Eur. J. Org. Chem. (2003) 2314
    • (2003) Eur. J. Org. Chem. , pp. 2314
    • Chicharro, R.1    de Castro, S.2    Reino, J.L.3    Aran, V.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.