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Volumn 9, Issue 5, 2007, Pages 943-945

Organocatalytic highly enantioselective nitroaldol reaction of α-ketophosphonates and nitromethane

Author keywords

[No Author keywords available]

Indexed keywords

DRUG DERIVATIVE; METHANE; NITROALKANE; NITROGEN; NITROMETHANE; PHOSPHORUS;

EID: 33947147190     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol070209i     Document Type: Article
Times cited : (127)

References (28)
  • 1
    • 33947159917 scopus 로고    scopus 로고
    • For reviews, see: a, 2nd ed, Juaristi, E, Soloshonok, V. A, Eds, John Wiley: Hoboken
    • For reviews, see: (a) Enantioselective Synthesis of β-Amino Acids, 2nd ed.; Juaristi, E., Soloshonok, V. A., Eds.; John Wiley: Hoboken, 2005.
    • (2005) Enantioselective Synthesis of β-Amino Acids
  • 4
    • 84891299621 scopus 로고    scopus 로고
    • Palacios, F.; Alonso, C.; de los Santos, J. In Enantioselective Synthesis of β-Amino Acids, 2nd ed.; Juaristi, E., Soloshonok, V. A., Eds.; John Wiley: Hoboken, 2005; Chapter 13, pp 277-318.
    • (b) Palacios, F.; Alonso, C.; de los Santos, J. In Enantioselective Synthesis of β-Amino Acids, 2nd ed.; Juaristi, E., Soloshonok, V. A., Eds.; John Wiley: Hoboken, 2005; Chapter 13, pp 277-318.
  • 5
    • 17144416365 scopus 로고    scopus 로고
    • For a review on naturally occurring β-amino-α- hydroxyphosphonic acid derivatives, see:, Kukhar, V. P, Hudson, H. R, Eds, John Wiley: Chichester
    • For a review on naturally occurring β-amino-α- hydroxyphosphonic acid derivatives, see: Mastałerz, P.; Kafarski, P. In Aminophosphonic and Aminophosphinic Acids-Chemistry and Biological Activity; Kukhar, V. P., Hudson, H. R., Eds.; John Wiley: Chichester, 2000; pp 1-31.
    • (2000) Aminophosphonic and Aminophosphinic Acids-Chemistry and Biological Activity , pp. 1-31
    • Mastałerz, P.1    Kafarski, P.2
  • 14
    • 8444252168 scopus 로고    scopus 로고
    • For a recent review on the asymmetric nitroaldol reactions, see
    • For a recent review on the asymmetric nitroaldol reactions, see: Palomo, C.; Oiarbide, M.; Mielgo, A. Angew. Chem., Int. Ed. 2004, 43, 5442-5444.
    • (2004) Angew. Chem., Int. Ed , vol.43 , pp. 5442-5444
    • Palomo, C.1    Oiarbide, M.2    Mielgo, A.3
  • 19
    • 31444439419 scopus 로고    scopus 로고
    • For examples of alkaloid-catalyzed asymmetric nitroaldol reactions, see: (a) Li, H, Wang, B, Deng, L. J. Am. Chem. Soc. 2006, 128, 732-733
    • For examples of alkaloid-catalyzed asymmetric nitroaldol reactions, see: (a) Li, H.; Wang, B.; Deng, L. J. Am. Chem. Soc. 2006, 128, 732-733.
  • 22
    • 0033549552 scopus 로고    scopus 로고
    • For an example of phase-transfer catalysis, see
    • For an example of phase-transfer catalysis, see: Corey, E. J.; Zang, F. Y. Angew. Chem., Int. Ed. 1999, 38, 1931-1934.
    • (1999) Angew. Chem., Int. Ed , vol.38 , pp. 1931-1934
    • Corey, E.J.1    Zang, F.Y.2
  • 23
    • 4143054678 scopus 로고    scopus 로고
    • For a review, see
    • For a review, see: Ooi, T.; Maruoka, K. Acc. Chem. Res. 2004, 37, 526-533.
    • (2004) Acc. Chem. Res , vol.37 , pp. 526-533
    • Ooi, T.1    Maruoka, K.2
  • 24
    • 4043154104 scopus 로고    scopus 로고
    • The C6′-OH has been shown to be essential for achieving high enantioselectivity in other reactions, too. For examples, see: (a) Li, H.; Wang, Y.; Tang, L.; Deng, L. J. Am. Chem. Soc. 2004, 126, 9906-9907.
    • The C6′-OH has been shown to be essential for achieving high enantioselectivity in other reactions, too. For examples, see: (a) Li, H.; Wang, Y.; Tang, L.; Deng, L. J. Am. Chem. Soc. 2004, 126, 9906-9907.
  • 28
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    • Ref 11a
    • (e) Ref 11a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.