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Volumn 72, Issue 5, 2007, Pages 1737-1741

Preparation and reactivity of versatile α-amino ketones

Author keywords

[No Author keywords available]

Indexed keywords

AMINES; AMINO ACIDS; FUNCTIONAL GROUPS; MOLECULAR ORIENTATION; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 33847625404     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo062401o     Document Type: Article
Times cited : (12)

References (24)
  • 6
    • 33847638624 scopus 로고    scopus 로고
    • Unpublished results
    • Yu, L.; Yudin, A. K. Unpublished results.
    • Yu, L.1    Yudin, A.K.2
  • 7
    • 0030818780 scopus 로고    scopus 로고
    • For examples of synthesis of N-protected aziridine Weinreb amides see: (a) Molander, G. A, Stengel, P. J. Tetrahedron 1997, 53, 8887-8912
    • For examples of synthesis of N-protected aziridine Weinreb amides see: (a) Molander, G. A.; Stengel, P. J. Tetrahedron 1997, 53, 8887-8912.
  • 13
    • 0012397313 scopus 로고
    • and references cited therein
    • (b) Snieckus, V. Chem. Rev. 1990, 90, 879-933 and references cited therein.
    • (1990) Chem. Rev , vol.90 , pp. 879-933
    • Snieckus, V.1
  • 14
    • 33845500079 scopus 로고    scopus 로고
    • The complications arise from undesired condensation chemistry. For a recent example of an amine-promoted aziridination of chalcones, see
    • The complications arise from undesired condensation chemistry. For a recent example of an amine-promoted aziridination of chalcones, see: Shen, Y.-M.; Zhao, M.-X.; Xu, J.; Shi, Y. Angew. Chem. Int. Ed. 2006, 45, 8005.
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 8005
    • Shen, Y.-M.1    Zhao, M.-X.2    Xu, J.3    Shi, Y.4
  • 22
    • 33847661257 scopus 로고    scopus 로고
    • The sample was heated in an NMR tube after addition of pyridine and cooled to room temperature prior to acquiring the spectrum
    • The sample was heated in an NMR tube after addition of pyridine and cooled to room temperature prior to acquiring the spectrum.
  • 24
    • 0001517130 scopus 로고    scopus 로고
    • The barrier to inversion in N-methylethylene imine is 19 kcal/mol, whereas the barrier to inversion in trimethylamine is 7.5 kcal/mol. See: Nielsen, I. M. B. J. Phys. Chem. A 1998, 102, 3193.
    • The barrier to inversion in N-methylethylene imine is 19 kcal/mol, whereas the barrier to inversion in trimethylamine is 7.5 kcal/mol. See: Nielsen, I. M. B. J. Phys. Chem. A 1998, 102, 3193.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.