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Volumn 70, Issue 9, 2005, Pages 3542-3553

Multicomponent synthesis of 2-imidazolines

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDES; AMINES; CATALYSIS; CHEMICAL ANALYSIS; COMPLEXATION; CYANIDES; KETONES; SUBSTITUTION REACTIONS;

EID: 20244384429     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo050132g     Document Type: Article
Times cited : (150)

References (62)
  • 2
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    • Dardonville, C.1    Rozas, I.2
  • 10
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    • Bousquet, P.; Feldman, J. Drugs 1999, 68, 799-812. Touzeau, F.; Arrault, A.; Guillaumet, G.; Scalbert, E.; Pfeiffer, B.; Rettori, M.-C.; Renard, P.; Mérour, J.-Y. J. Med. Chem. 2003, 46, 1962-1979.
    • (1999) Drugs , vol.68 , pp. 799-812
    • Bousquet, P.1    Feldman, J.2
  • 20
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    • (a) An example is the development of ruthenium-based metathesis catalysts. For a review on this subject, see: Trnka, T.; Grubbs, R. H. Acc. Chem. Res. 2001, 34, 18-29.
    • (2001) Acc. Chem. Res. , vol.34 , pp. 18-29
    • Trnka, T.1    Grubbs, R.H.2
  • 21
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    • and references therein
    • (b) For a review on NHC ligands in homogeneous catalysis, see: Herrmann, W. A. Angew. Chem., Int. Ed. 2002, 41, 1290-1309 and references therein.
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 1290-1309
    • Herrmann, W.A.1
  • 32
    • 2542519356 scopus 로고    scopus 로고
    • The first example of a rhodium-catalyzed direct C-H insertion of 4,4-dimethyl-2-imidazoline to 3,3-dimethylbut-1-ene was reported in: Wiedemann, S. H.; Bergman, R. G.; Ellman, J. A. Org. Lett. 2004, 6, 1685-1687.
    • (2004) Org. Lett. , vol.6 , pp. 1685-1687
    • Wiedemann, S.H.1    Bergman, R.G.2    Ellman, J.A.3
  • 35
    • 0002654769 scopus 로고
    • For examples see: (a) Fehlhammer, W. P.; Bartel, K.; Petri, W. J. Organomet. Chem. 1975, 87, C34-C36. (b) Fehlhammer, W. P.; Zinner, G.; Bakola-Christianopoulou, M. J. Organomet. Chem. 1987, 331, 193-205.
    • (1975) J. Organomet. Chem. , vol.87
    • Fehlhammer, W.P.1    Bartel, K.2    Petri, W.3
  • 42
    • 17744364664 scopus 로고    scopus 로고
    • note
    • A second byproduct, isolated in only 7%, was characterized as the oxazoline formed by reaction of 25a and 10.
  • 49
    • 0344887064 scopus 로고
    • a of 4b in DMSO (25°C) is 12.3, see: Bordwell, F. G. Acc. Chem. Res. 1988, 21, 456-463.
    • (1988) Acc. Chem. Res. , vol.21 , pp. 456-463
    • Bordwell, F.G.1
  • 52
    • 17744390751 scopus 로고    scopus 로고
    • note
    • 4, see ref 36b) resulted in even higher yields for 50a (42%) and 50b (33%).
  • 56
    • 17744368858 scopus 로고    scopus 로고
    • SCM, Theoretical Chemistry, Vrije Universiteit, Amsterdam, The Netherlands
    • (c) ADF 2004.01; SCM, Theoretical Chemistry, Vrije Universiteit, Amsterdam, The Netherlands, http://www.scm.com.
    • ADF 2004.01
  • 61
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    • Erratum: Perdew, J. P. Phys. Rev. B 1986, 34, 7406-7406
    • Perdew, J. P. Phys. Rev. B 1986, 33, 8822-8824. Erratum: Perdew, J. P. Phys. Rev. B 1986, 34, 7406-7406.
    • (1986) Phys. Rev. B , vol.33 , pp. 8822-8824
    • Perdew, J.P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.