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Volumn 9, Issue 6, 2007, Pages 1149-1151

Catalytic asymmetric three-component acyl-strecker reaction

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; AMIDE; AMINE; AMINO ACID; CYANIDE; IMINE; NITRILE; THIOUREA;

EID: 33947581412     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0702674     Document Type: Article
Times cited : (101)

References (51)
  • 1
    • 0041378065 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Gröger, H. Chem. Rev. 2003, 103, 2795-2827.
    • (2003) Chem. Rev , vol.103 , pp. 2795-2827
    • Gröger, H.1
  • 24
    • 33845625404 scopus 로고
    • For alternative non-enantioselective variants, see: a
    • For alternative non-enantioselective variants, see: (a) Dornow, A.; Lupfert, S. Chem. Ber. 1956, 89, 2718-2722.
    • (1956) Chem. Ber , vol.89 , pp. 2718-2722
    • Dornow, A.1    Lupfert, S.2
  • 26
    • 33947609485 scopus 로고
    • U.S. patent 2849477
    • (c) Dornow, A.; Lüpfert, S. U.S. patent 2849477, 1958.
    • (1958)
    • Dornow, A.1    Lüpfert, S.2
  • 39
    • 23944488799 scopus 로고    scopus 로고
    • For the first use of acetyl cyanide in an acylcyanation of aldehydes, see: j
    • For the first use of acetyl cyanide in an acylcyanation of aldehydes, see: (j) Lundgren, S.; Wingstrand, E.; Penhoat, M.; Moberg, C. J. Am. Chem. Soc. 2005, 127, 11592-11593.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 11592-11593
    • Lundgren, S.1    Wingstrand, E.2    Penhoat, M.3    Moberg, C.4
  • 43
    • 0346865819 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Schreiner, P. R. Chem. Soc. Rev. 2003, 32, 289-296.
    • (2003) Chem. Soc. Rev , vol.32 , pp. 289-296
    • Schreiner, P.R.1
  • 49
    • 84890734483 scopus 로고    scopus 로고
    • For a review on catalytic asymmetric multicomponent reactions, see:, Zhu, J, Bienaymé, H, Eds, WILEY-VCH: Weinheim, Germany
    • For a review on catalytic asymmetric multicomponent reactions, see: Seayad, J.; List, B. In Multicomponent Reactions; Zhu, J., Bienaymé, H., Eds.; WILEY-VCH: Weinheim, Germany, 2005; pp 277-298.
    • (2005) Multicomponent Reactions , pp. 277-298
    • Seayad, J.1    List, B.2
  • 50
    • 33947589590 scopus 로고    scopus 로고
    • If HCN was used rather than acetyl cyanide, under the same reaction conditions, following standard in situ derivatization with trifluoroacetic acid anhydride, the obtained product was essentially racemic
    • If HCN was used rather than acetyl cyanide, under the same reaction conditions, following standard in situ derivatization with trifluoroacetic acid anhydride, the obtained product was essentially racemic.
  • 51
    • 33947606465 scopus 로고    scopus 로고
    • No conversion was obtained when cyanoformate esters or benzoylcyanide were used as the cyanide source
    • No conversion was obtained when cyanoformate esters or benzoylcyanide were used as the cyanide source.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.