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Volumn 9, Issue 10, 2007, Pages 1943-1946

Highly enantioselective α-aminoxylation of aldehydes and ketones with a polymer-supported organocatalyst

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; CYCLOHEXANONE; CYCLOHEXANONE DERIVATIVE; KETONE; NITROGEN; OXYGEN; POLYMER; PROLINE;

EID: 34249297939     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol070526p     Document Type: Article
Times cited : (125)

References (29)
  • 11
    • 7444257444 scopus 로고    scopus 로고
    • Mechanistic studies: (a) Cheong, P. H.-Y.; Houk, K. N. J. Am. Chem. Soc. 2004, 126, 13912.
    • Mechanistic studies: (a) Cheong, P. H.-Y.; Houk, K. N. J. Am. Chem. Soc. 2004, 126, 13912.
  • 15
    • 0141619399 scopus 로고    scopus 로고
    • For reviews on immobilized organocatalysts, see: a
    • For reviews on immobilized organocatalysts, see: (a) Benaglia, M.; Puglisi, A.; Cozzi, F. Chem. Rev. 2003, 103, 3401.
    • (2003) Chem. Rev , vol.103 , pp. 3401
    • Benaglia, M.1    Puglisi, A.2    Cozzi, F.3
  • 24
    • 33746690372 scopus 로고    scopus 로고
    • For a different strategy towards catalyst recovery in this reaction, involving the use of ionic liquids, see: a
    • For a different strategy towards catalyst recovery in this reaction, involving the use of ionic liquids, see: (a) Guo, H.-M.; Niu, H.-Y.; Xue, M.-X.; Guo, Q.-X.; Cun, L.-F.; Mi, A.-Q.; Jiang, Y.-Z.; Wang, J.-J. Green Chem. 2006, 8, 682.
    • (2006) Green Chem , vol.8 , pp. 682
    • Guo, H.-M.1    Niu, H.-Y.2    Xue, M.-X.3    Guo, Q.-X.4    Cun, L.-F.5    Mi, A.-Q.6    Jiang, Y.-Z.7    Wang, J.-J.8
  • 27
    • 34249286699 scopus 로고    scopus 로고
    • 1H NMR spectra of the reaction crudes (in DMF and DMSO) showed small signals due to the formation of the α, α′-bisaminoxylation product which was not observed using chloroform.
    • 1H NMR spectra of the reaction crudes (in DMF and DMSO) showed small signals due to the formation of the α, α′-bisaminoxylation product which was not observed using chloroform.
  • 28
    • 34249334705 scopus 로고    scopus 로고
    • An experiment in DMF with the conditions of entry 1 (Table 2) showed, after 7 h, no progress of the reaction
    • An experiment in DMF with the conditions of entry 1 (Table 2) showed, after 7 h, no progress of the reaction.
  • 29
    • 0037134880 scopus 로고    scopus 로고
    • For examples of self-aldolization of aldehydes, see: Northrup, A, MacMillan, D. W. C. J. Am. Chem. Soc. 2002, 124, 6798
    • For examples of self-aldolization of aldehydes, see: Northrup, A.; MacMillan, D. W. C. J. Am. Chem. Soc. 2002, 124, 6798.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.