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Volumn 13, Issue 9, 2011, Pages 2464-2467

A dual-catalysis/anion-binding approach to the kinetic resolution of allylic amines

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; ANION;

EID: 79955604602     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol200712b     Document Type: Article
Times cited : (81)

References (110)
  • 46
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    • Enzymatic preparations of nonracemic amines
    • Enzymatic preparations of nonracemic amines: Paetzold, J.; Bäckvall, J. E. J. Am. Chem. Soc. 2005, 127, 17620
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 17620
    • Paetzold, J.1    Bäckvall, J.E.2
  • 61
    • 0033921576 scopus 로고    scopus 로고
    • For reviews on nucleophilic/Lewis base catalysis, see
    • For reviews on nucleophilic/Lewis base catalysis, see: Fu, G. C. Acc. Chem. Res. 2000, 33, 412
    • (2000) Acc. Chem. Res. , vol.33 , pp. 412
    • Fu, G.C.1
  • 75
    • 28944449340 scopus 로고    scopus 로고
    • For examples of anion-binding approaches to catalysis, see
    • For examples of anion-binding approaches to catalysis, see: Kotke, M.; Schreiner, P. R. Tetrahedron 2006, 62, 434
    • (2006) Tetrahedron , vol.62 , pp. 434
    • Kotke, M.1    Schreiner, P.R.2
  • 87
    • 0001708390 scopus 로고
    • For other examples of chiral anion catalysis, see
    • For other examples of chiral anion catalysis, see: Alper, H.; Hamel, N. J. Am. Chem. Soc. 1990, 112, 2803
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 2803
    • Alper, H.1    Hamel, N.2
  • 103
    • 85050296727 scopus 로고
    • s factor = rate of faster reacting enantiomer/rate of slower reacting enantiomer. s factors were calculated according to:;, See the Supporting Information for details
    • s factor = rate of faster reacting enantiomer/rate of slower reacting enantiomer. s factors were calculated according to: Kagan, H. B.; Fiaud, J. C. Top. Stereochem. 1988, 18, 249 See the Supporting Information for details
    • (1988) Top. Stereochem. , vol.18 , pp. 249
    • Kagan, H.B.1    Fiaud, J.C.2
  • 109
    • 0742324457 scopus 로고    scopus 로고
    • The requisite racemic allylic amines were conveniently obtained in one step from the corresponding α,β-unsaturated ketones by following a modified literature procedure:;;, See the Supporting Information for details.
    • The requisite racemic allylic amines were conveniently obtained in one step from the corresponding α,β-unsaturated ketones by following a modified literature procedure: Miriyala, B.; Bhattacharyya, S.; Williamson, J. S. Tetrahedron 2004, 60, 1463 See the Supporting Information for details.
    • (2004) Tetrahedron , vol.60 , pp. 1463
    • Miriyala, B.1    Bhattacharyya, S.2    Williamson, J.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.