메뉴 건너뛰기




Volumn 65, Issue 34, 2009, Pages 6991-7000

Selective synthesis of α-trifluoromethyl-β-aryl enamines or vinylogous guanidinium salts by treatment of β-halo-β-trifluoromethylstyrenes with secondary amines under different conditions

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA TRIFLUOROMETHYL BETA ARYL ENAMINE DERIVATIVE; AMINE; BETA HALO BETA TRIFLUOROMETHYLSTYRENE DERIVATIVE; ENAMINE; GUANIDINE DERIVATIVE; SOLVENT; STYRENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 67650561446     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.06.048     Document Type: Article
Times cited : (39)

References (85)
  • 10
    • 67650546909 scopus 로고    scopus 로고
    • Ojima I., McCarthy J.R., and Welch J.T. (Eds), American Chemical Society, Washington, DC
    • In: Ojima I., McCarthy J.R., and Welch J.T. (Eds). Biomedical Frontiers of Fluorine Chemistry. ACS Symposium Series 639 (1996), American Chemical Society, Washington, DC
    • (1996) ACS Symposium Series 639
  • 11
    • 4544321125 scopus 로고    scopus 로고
    • Fluorine in the Life Sciences, Multiauthor Special Issue
    • Fluorine in the Life Sciences, Multiauthor Special Issue. ChemBioChem 5 (2004) 559-722
    • (2004) ChemBioChem , vol.5 , pp. 559-722
  • 12
    • 33644909264 scopus 로고    scopus 로고
    • Fluorine in the Life Science Industry, Multiauthor Special Issue
    • Fluorine in the Life Science Industry, Multiauthor Special Issue. Chimia 58 (2004) 92-162
    • (2004) Chimia , vol.58 , pp. 92-162
  • 13
    • 49849105560 scopus 로고    scopus 로고
    • Fluorine-Containing Agrochemicals: An Overview of Recent Developments
    • Tressaud A. (Ed), Elsevier, Amsterdam
    • Theodoridis G. Fluorine-Containing Agrochemicals: An Overview of Recent Developments. In: Tressaud A. (Ed). Advances in Fluorine Science Vol. 2 (2006), Elsevier, Amsterdam 121-175
    • (2006) Advances in Fluorine Science , vol.2 , pp. 121-175
    • Theodoridis, G.1
  • 16
    • 0041788267 scopus 로고
    • Chemistry of Organic Fluorine Compounds II
    • American Chemical Society, Washington, DC
    • Hudlický M., and Pavlath A.P. Chemistry of Organic Fluorine Compounds II. ACS Symposium Series 187 (1995), American Chemical Society, Washington, DC
    • (1995) ACS Symposium Series 187
    • Hudlický, M.1    Pavlath, A.P.2
  • 18
    • 67650528736 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
  • 19
    • 67650555363 scopus 로고    scopus 로고
    • Soloshonok V.A. (Ed), American Chemical Society, Washington, DC
    • In: Soloshonok V.A. (Ed). Fluorine-Containing Synthons. ACS Symposium Series 911 (2005), American Chemical Society, Washington, DC
    • (2005) ACS Symposium Series 911
  • 20
    • 49849099200 scopus 로고    scopus 로고
    • Percy J.M. (Ed), Thieme, Stuttgart
    • In: Percy J.M. (Ed). Science of Synthesis. Fluorine Vol. 34 (2006), Thieme, Stuttgart
    • (2006) Fluorine , vol.34
  • 21
    • 67650561128 scopus 로고    scopus 로고
    • Soloshonok V.A., Mikami K., Yamazaki T., Welch J.T., and Honek J.F. (Eds), American Chemical Society, Washington, DC
    • In: Soloshonok V.A., Mikami K., Yamazaki T., Welch J.T., and Honek J.F. (Eds). Current Fluoroorganic Chemistry. New Synthetic Directions, Technologies, Materials, and Biological Applications. ACS Symposium Series 949 (2006), American Chemical Society, Washington, DC
    • (2006) ACS Symposium Series 949
  • 51
    • 57249090592 scopus 로고    scopus 로고
    • Russ. Chem. Rev. 71 (2002) 195-221
    • (2002) Russ. Chem. Rev. , vol.71 , pp. 195-221
  • 69
    • 67650546908 scopus 로고    scopus 로고
    • Baasner B., Hagemann H., and Tatlow J.C. (Eds), Georg Thieme, Stuttgart
    • Welch J.T. In: Baasner B., Hagemann H., and Tatlow J.C. (Eds). Methods of Organic Chemistry (Houben-Weyl) Vol. E10b/2 (2000), Georg Thieme, Stuttgart 382-459
    • (2000) Methods of Organic Chemistry (Houben-Weyl) , vol.E10b-2 , pp. 382-459
    • Welch, J.T.1
  • 73
    • 67650563846 scopus 로고    scopus 로고
    • NV mechanism see:
    • NV mechanism see:
  • 80
    • 84918171920 scopus 로고
    • Russ. Chem. Rev. 55 (1986) 511-530
    • (1986) Russ. Chem. Rev. , vol.55 , pp. 511-530
  • 82
    • 0005798222 scopus 로고    scopus 로고
    • Russ. Chem. Rev. 67 (1998) 279-293
    • (1998) Russ. Chem. Rev. , vol.67 , pp. 279-293


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.