메뉴 건너뛰기




Volumn 19, Issue 14, 2008, Pages 1676-1683

Trifluoromethylation of camphorquinone and its monoimine derivatives

Author keywords

[No Author keywords available]

Indexed keywords

1,3 OXAZOLIDIN 2 ONE; 2 HYDROXY 2 (TRIFLUOROMETHYL)BORNAN 3 ONE; 3 IMINO 2 (TRIFLUOROMETHYL)BORNAN 2 OLS; ALCOHOL; AMINO ACID DERIVATIVE; BORNANE DERIVATIVE; CAMPHORQUINONE; CESIUM; IMINE; KETONE; OXAZOLIDINE DERIVATIVE; PHOSGENE; SILANE DERIVATIVE; TRIFLUOROMETHYLTRIMETHYLSILANE;

EID: 48349087440     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2008.07.003     Document Type: Article
Times cited : (14)

References (62)
  • 12
    • 48349135806 scopus 로고    scopus 로고
    • Ramachandran P.V. (Ed), American Chemical Society, Washington, DC
    • In: Ramachandran P.V. (Ed). Asymmetric Fluoroorganic Chemistry: Synthesis, Applications, and Future Directions. ACS Symposium Series 746 (2000), American Chemical Society, Washington, DC
    • (2000) ACS Symposium Series 746
  • 34
    • 48349118709 scopus 로고    scopus 로고
    • note
    • 15.
  • 40
    • 48349093616 scopus 로고    scopus 로고
    • note
    • 17a.
  • 41
    • 48349124824 scopus 로고    scopus 로고
    • Johnson, C. K. ORTEP II, Report ORNL-5138, Oak Ridge National Laboratory, Oak Ridge, Tennessee, 1976.
    • Johnson, C. K. ORTEP II, Report ORNL-5138, Oak Ridge National Laboratory, Oak Ridge, Tennessee, 1976.
  • 43
    • 34249288615 scopus 로고    scopus 로고
    • 2O) led selectively to the reduction of the C{double bond, long}O group without deprotection (see: Fujiwara, K.; Aki, Y.; Yamamoto, F.; Kawamura, M.; Kobayashi, M.; Okano, A.; Awakura, D.; Shiga, S.; Murai, A.; Kawai, H.; Suzuki, T. Tetrahedron Lett. 2007, 26, 4523-4527).
    • 2O) led selectively to the reduction of the C{double bond, long}O group without deprotection (see: Fujiwara, K.; Aki, Y.; Yamamoto, F.; Kawamura, M.; Kobayashi, M.; Okano, A.; Awakura, D.; Shiga, S.; Murai, A.; Kawai, H.; Suzuki, T. Tetrahedron Lett. 2007, 26, 4523-4527).
  • 44
    • 48349096272 scopus 로고    scopus 로고
    • 2O/hexane) was prepared from rac-3a analogously to the enantiomerically pure 9a.
    • 2O/hexane) was prepared from rac-3a analogously to the enantiomerically pure 9a.
  • 45
    • 48349095608 scopus 로고    scopus 로고
    • note
    • 23c.
  • 52
    • 48349107368 scopus 로고    scopus 로고
    • note
    • It is worth mentioning that this signal appears as a d and not as the expected dd. This fact shows that the coupling occurs with only one H-atom located at C(5) of the camphor skeleton. It is likely that the effective coupling results from the interaction with the exo-H. The same phenomenon is observed in other camphor derivatives described in this paper.
  • 54
    • 48349134736 scopus 로고    scopus 로고
    • note
    • CCDC 684655-684657 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre, via www.ccdc.cam.ac.uk/data_request/cif.
  • 55
    • 0031059866 scopus 로고    scopus 로고
    • Carter Jr. C.W., and Sweet R.M. (Eds), Academic Press, New York
    • Otwinowski Z., and Minor W. In: Carter Jr. C.W., and Sweet R.M. (Eds). Methods in Enzymology. Macromolecular Crystallography, Part A Vol. 276 (1997), Academic Press, New York 307-326
    • (1997) Macromolecular Crystallography, Part A , vol.276 , pp. 307-326
    • Otwinowski, Z.1    Minor, W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.