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Volumn 73, Issue 6, 2008, Pages 2256-2263

Synthesis and intramolecular pericyclization of 1-azulenyl thioketones

Author keywords

[No Author keywords available]

Indexed keywords

AZULENE RING; HYDROGEN TRANSFER; INTRAMOLECULAR PERICYCLIZATION; INTRAMOLECULAR REACTION;

EID: 41849124566     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo702309b     Document Type: Article
Times cited : (25)

References (46)
  • 1
    • 0000840877 scopus 로고
    • Thiocarbonyl Compounds
    • Barton, D, Ollis, W. D, Jones, D. N, Eds, Pergamon: Oxford, UK
    • Duus, F. Thiocarbonyl Compounds. In Comprehensive Organic Chemistry; Barton, D., Ollis, W. D., Jones, D. N., Eds.; Pergamon: Oxford, UK, 1979; Vol. 3, pp 373-487.
    • (1979) Comprehensive Organic Chemistry , vol.3 , pp. 373-487
    • Duus, F.1
  • 5
    • 0000829582 scopus 로고
    • 4th ed, Kropf, H, Ed, Georg Thieme: Stuttgart, Germany
    • Zeller, K.-P. Azulene. In Houben-Weyl: Methoden der Organischen Chemie, 4th ed.; Kropf, H., Ed.; Georg Thieme: Stuttgart, Germany, 1985; Vol. V, Part 2C, pp 127-418.
    • (1985) Houben-Weyl: Methoden der Organischen Chemie , vol.5 , Issue.PART 2C , pp. 127-418
    • Zeller, K.-P.A.1
  • 39
    • 41849103018 scopus 로고    scopus 로고
    • The molecular orbital calculations were done with a Gaussian revision E.2 program package, which was installed in an UNIX workstation under a molecular design support system in IMRAM. Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Gill, P. M. W.; Johnson, B. G.; Robb, M. A.; Cheeseman, J. R.; Keith, T.; Petersson, G. A.; Montgomery, J. A.; Raghavachari, K.; Al-Laham, M. A.; Zakrzewski, V. G.; Ortiz, J. V.; Foresman, J. B.; Cioslowski, J.; Stefanov, B. B.; Nanayakkara, A.; Challacombe, M.; Peng, C. Y.; Ayala, P. Y.; Chen, W.; Wong, M. W.; Andres, J. L.; Replogle, E. S.; Gomperts, R.; Martin, R. L.; Fox, D. J.; Binkley, J. S.; Defrees, D. J.; Baker, J.; Stewart, J. P.; Head-Gordon, M.; Gonzalez, C.; Pople, J. A. Gaussian, revision E.2; Gaussian, Inc.: Pittsburgh, PA, 1995.
    • The molecular orbital calculations were done with a Gaussian revision E.2 program package, which was installed in an UNIX workstation under a molecular design support system in IMRAM. Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Gill, P. M. W.; Johnson, B. G.; Robb, M. A.; Cheeseman, J. R.; Keith, T.; Petersson, G. A.; Montgomery, J. A.; Raghavachari, K.; Al-Laham, M. A.; Zakrzewski, V. G.; Ortiz, J. V.; Foresman, J. B.; Cioslowski, J.; Stefanov, B. B.; Nanayakkara, A.; Challacombe, M.; Peng, C. Y.; Ayala, P. Y.; Chen, W.; Wong, M. W.; Andres, J. L.; Replogle, E. S.; Gomperts, R.; Martin, R. L.; Fox, D. J.; Binkley, J. S.; Defrees, D. J.; Baker, J.; Stewart, J. P.; Head-Gordon, M.; Gonzalez, C.; Pople, J. A. Gaussian, revision E.2; Gaussian, Inc.: Pittsburgh, PA, 1995.
  • 40
    • 41849096668 scopus 로고    scopus 로고
    • The B3LYP/6-31G** density functional calculations were performed by Spartan'04, Wavefunction, Inc.: Irvine, CA.
    • The B3LYP/6-31G** density functional calculations were performed by Spartan'04, Wavefunction, Inc.: Irvine, CA.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.