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Volumn 126, Issue 21, 2004, Pages 6558-6559

Catalytic asymmetric synthesis of α-amino phosphonates using enantioselective carbon-carbon bond-forming reactions

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA AMINO ACID; ALPHA AMINOPHOSPHONATE; CARBON; COPPER COMPLEX; HEXAFLUORO 2 PROPANOL; PHOSPHONIC ACID DERIVATIVE; PROTON; SILICON DERIVATIVE; UNCLASSIFIED DRUG;

EID: 2542556554     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja048791i     Document Type: Article
Times cited : (101)

References (26)
  • 7
    • 2142811043 scopus 로고    scopus 로고
    • Kukhar, V. P., Hudson, H. R., Eds.; John Wiley and Sons; Chapter 5
    • For review, (f) Kukhar, V. P. In Aminophosphonic and Aminophosphinic Acids; Kukhar, V. P., Hudson, H. R., Eds.; John Wiley and Sons: 2000; Chapter 5, p 127.
    • (2000) Aminophosphonic and Aminophosphinic Acids , pp. 127
    • Kukhar, V.P.1
  • 14
    • 1842555199 scopus 로고    scopus 로고
    • After submitting this manuscript, Jacobsen et al. have reported catalytic enantioselective hydrophosphonylation of imines: (m) Joly, G. D.; Jacobsen, E. N. J. Am. Chem. Soc. 2004, 126, 4102.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 4102
    • Joly, G.D.1    Jacobsen, E.N.2
  • 17
    • 0030781212 scopus 로고    scopus 로고
    • For examples where HFIP was used in catalytic asymmetric reactions, see: (a) Kitajima, H.; Ito, K.; Katsuki, T. Tetrahedron 1997, 53, 17015.
    • (1997) Tetrahedron , vol.53 , pp. 17015
    • Kitajima, H.1    Ito, K.2    Katsuki, T.3
  • 19
    • 2542600296 scopus 로고    scopus 로고
    • note
    • Experimental details are shown in the Supporting Information.
  • 25
    • 2542607869 scopus 로고    scopus 로고
    • note
    • Preliminary biological tests have shown that 8g and 8j have low activity for inhibition of kynureninase and kynurenine 3-hydroxylase. We thank Dr. Kuniaki Saito (Gifu University) for measurements of the biological activity of 8g and 8j.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.