메뉴 건너뛰기




Volumn 53, Issue 7, 2012, Pages 752-757

An original route to newly-functionalized indoles and carbazoles starting from the ring-opening of nitrothiophenes

Author keywords

Carbazoles; Indoles; Michael type additions; Nitrobutadienes; Nitrogen heterocycles

Indexed keywords

1,3 BUTADIENE DERIVATIVE; CARBAZOLE DERIVATIVE; FUSED CARBON NITROGEN HETEROCYCLE; INDOLE DERIVATIVE; THIOPHENE DERIVATIVE;

EID: 84855825950     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.11.137     Document Type: Article
Times cited : (20)

References (47)
  • 7
    • 84884908849 scopus 로고    scopus 로고
    • 2,3-Dinitro-1,3-butadienes: Versatile Building Blocks from the Ring Opening of 3,4-Dinitrothiophene
    • Attanasi, O. A., Spinelli, D., Eds.; Società Chimica Italiana: Rome
    • (a) Bianchi, L.; Maccagno, M.; Petrillo, G.; Sancassan, F.; Spinelli, D.; Tavani, C. 2,3-Dinitro-1,3-butadienes: Versatile Building Blocks from the Ring Opening of 3,4-Dinitrothiophene In Targets in Heterocyclic Systems: Chemistry and Properties; Attanasi, O. A., Spinelli, D., Eds.; Società Chimica Italiana: Rome, 2006; Vol. 10, pp 1–23
    • (2006) Targets in Heterocyclic Systems: Chemistry and Properties , vol.10 , pp. 1-23
    • Bianchi, L.1    Maccagno, M.2    Petrillo, G.3    Sancassan, F.4    Spinelli, D.5    Tavani, C.6
  • 8
    • 0008694074 scopus 로고    scopus 로고
    • Synthetic Exploitation of the Ring-Opening of 3,4-Dinitrothiophene
    • Attanasi, O. A., Spinelli, D., Eds.; Research Signpost: Trivandrum, India
    • (b) DellErba, C.; Novi, M.; Petrillo, G.; Tavani, C. Synthetic Exploitation of the Ring-Opening of 3,4-Dinitrothiophene In Topics in Heterocyclic Systems: Synthesis Reactions and Properties; Attanasi, O. A., Spinelli, D., Eds.; Research Signpost: Trivandrum, India, 1996; Vol. 1, pp 1–12.
    • (1996) Topics in Heterocyclic Systems: Synthesis Reactions and Properties , vol.1 , pp. 1-12
    • Dellerba, C.1    Novi, M.2    Petrillo, G.3    Tavani, C.4
  • 22
    • 76549119703 scopus 로고    scopus 로고
    • Ring-opening/ring-closing protocols from nitrothiophenes: Six-membered versus unusual eight-membered sulfur heterocycles through michael-type addition on nitrobutadienes
    • Bianchi, L.; Giorgi, G.; Maccagno, M.; Petrillo, G.; Sancassan, F.; Severi, E.; Spinelli, D.; Stenta, M.; Tavani, C. Ring-opening/ring-closing protocols from nitrothiophenes: Six-membered versus unusual eight-membered sulfur heterocycles through michael-type addition on nitrobutadienes. Chemistry - A European Journal, Volume 16, Issue 4, 2010, Pages 1312-1318. doi: 10.1002/chem.200902528.
    • (2010) Chemistry - a European Journal , vol.16 , Issue.4 , pp. 1312-1318
    • Bianchi, L.1    Giorgi, G.2    Maccagno, M.3    Petrillo, G.4    Sancassan, F.5    Severi, E.6    Spinelli, D.7    Stenta, M.8    Tavani, C.9
  • 27
    • 84943388739 scopus 로고
    • Pyrroles and their Benzoderivatives: Synthesis and Applications
    • Katritzky, A. R., Rees, C. W., Eds.; Pergamon: Oxford
    • (a) Sundberg, R. J. Pyrroles and their Benzoderivatives: Synthesis and Applications In Comprehensive Heterocyclic Chemistry; Katritzky, A. R., Rees, C. W., Eds.; Pergamon: Oxford, 1984; Vol. 4, pp 313–376
    • (1984) Comprehensive Heterocyclic Chemistry , vol.4 , pp. 313-376
    • Sundberg, R.J.1
  • 33
    • 85077096433 scopus 로고    scopus 로고
    • 3): d (ppm) 21.09, 39.72, 110.98, 119.15, 119.85, 119.93, 121.84, 123.53, 127.04, 128.53, 128.89, 135.47, 136.63, 140.92
    • 3): d (ppm) 21.09, 39.72, 110.98, 119.15, 119.85, 119.93, 121.84, 123.53, 127.04, 128.53, 128.89, 135.47, 136.63, 140.92.
  • 40
    • 85077103200 scopus 로고    scopus 로고
    • +], 407(7), 374(9), 361(20), 345(20), 332(17), 316(12), 255(9), 171(16), 164(63), 158(51), 151(34), 146 (28), 138(14), 119(10), 91(12)
    • •], 407(7), 374(9), 361(20), 345(20), 332(17), 316(12), 255(9), 171(16), 164(63), 158(51), 151(34), 146 (28), 138(14), 119(10), 91(12).
  • 41
    • 85077098123 scopus 로고    scopus 로고
    • 35 Crystallographic data (excluding structure factors) for structure 19b have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication No. CCDC-836410. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK, (fax: +44 (0) 1223 336033 or e-mail: deposit@ccdc.cam.ac.uk)
    • 35 Crystallographic data (excluding structure factors) for structure 19b have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication No. CCDC-836410. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK, (fax: +44 (0) 1223 336033 or e-mail: deposit@ccdc.cam.ac.uk).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.