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Volumn , Issue , 2005, Pages 487-501

Enantiopure amines by chirality transfer using (R)-Phenylglycine amide

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EID: 84885776170     PISSN: None     EISSN: None     Source Type: Book    
DOI: None     Document Type: Chapter
Times cited : (2)

References (71)
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    • Eur. Pat. Appl. EP 442584
    • Boesten, W. H. J. Eur. Pat. Appl. EP 442584, 1991.
    • (1991)
    • Boesten, W.H.J.1
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    • 85130570542 scopus 로고
    • Eur. Pat. Appl. EP 442585
    • Boesten, W. H. J. Eur. Pat. Appl. EP 442585, 1991.
    • (1991)
    • Boesten, W.H.J.1
  • 18
    • 0001249611 scopus 로고
    • Helmchen, G., Hoffmann, R. W., Mulzer, J., Schaumann, E., Eds., Vol. E 21, D.1.4.4., Thieme Verlag, Stuttgart
    • Kunz, H. in Houben-Weyl: Stereoselective Synthesis, Helmchen, G., Hoffmann, R. W., Mulzer, J., Schaumann, E., Eds., Vol. E 21, D.1.4.4., Thieme Verlag, Stuttgart, 1995, 1931.
    • (1995) Houben-Weyl: Stereoselective Synthesis , pp. 1931
    • Kunz, H.1
  • 27
    • 0001353976 scopus 로고
    • Few examples of crystallization-induced asymmetric transformations in Strecker reactions based on arylalkyl-methyl ketones have been reported: Weinges, K., Gries, K., Stemmle, B., Schrank, W. Chem. Ber. 1977, 110, 2098.
    • (1977) Chem. Ber , vol.110 , pp. 2098
  • 33
    • 85130522251 scopus 로고    scopus 로고
    • HCN can be used at large scale
    • HCN can be used at large scale.
  • 34
    • 85130510891 scopus 로고    scopus 로고
    • For example, in the case of phenylacetone, it was found that in solution the initially formed minor isomer preferentially precipitated under crystallization conditions
    • For example, in the case of phenylacetone, it was found that in solution the initially formed minor isomer preferentially precipitated under crystallization conditions.
  • 41
    • 85130568674 scopus 로고    scopus 로고
    • Two isomers in a ratio of 1:1.3 were obtained for the additional methyl group present in the crotyl moiety
    • Two isomers in a ratio of 1:1.3 were obtained for the additional methyl group present in the crotyl moiety.
  • 50
    • 0003491440 scopus 로고
    • Georg Thieme Verlag, Band E5
    • Houben Weyl series, Methoden der Organischen Chemie, Georg Thieme Verlag, 1985, Band E5, p. 259.
    • (1985) Methoden der Organischen Chemie , pp. 259
  • 55
    • 85130523730 scopus 로고    scopus 로고
    • Using (S)-PGA as the chiral auxiliary would yield (R)-1-aminoindane or, (R)-3,3-dimethyl-2-buty-lamine, respectively
    • Using (S)-PGA as the chiral auxiliary would yield (R)-1-aminoindane or, (R)-3,3-dimethyl-2-buty-lamine, respectively.
  • 58
    • 85130551987 scopus 로고    scopus 로고
    • W.O. Patent 96/21640
    • Lidor, R., Bahar, E. W.O. Patent 96/21640, 1996.
    • (1996)
    • Lidor, R.1    Bahar, E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.