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Volumn 52, Issue 1, 2011, Pages 129-132

Direct Leuckart-type reductive amination of aldehydes and ketones: A facile one-pot protocol for the preparation of secondary and tertiary amines

Author keywords

Aldehydes; Ketones; Reductive amination; Secondary amines; Tertiary amines

Indexed keywords

ALDEHYDE DERIVATIVE; AMINE; KETONE DERIVATIVE; TERTIARY AMINE;

EID: 78649854588     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.11.006     Document Type: Article
Times cited : (40)

References (57)
  • 1
    • 78649874217 scopus 로고    scopus 로고
    • In a leading article by Abdel-Magid, et al. (Ref. 7a) reductive amination is 'described as a direct reaction when the carbonyl compound and the amine are mixed with the proper reducing agent without prior formation of the intermediate imine or iminium salt
    • In a leading article by Abdel-Magid, et al. (Ref. 7a) reductive amination is 'described as a direct reaction when the carbonyl compound and the amine are mixed with the proper reducing agent without prior formation of the intermediate imine or iminium salt.'
  • 3
    • 0000856963 scopus 로고
    • W.S. Emerson R. Adams, Organic Reactions Vol. V 1948 John Wiley & Sons New York 174 255
    • (1948) Organic Reactions , vol.5 , pp. 174-255
    • Emerson, W.S.1
  • 10
    • 85068666190 scopus 로고
    • For a review on sodium cyanoborohydride, see: C.F. Lane Synthesis 1975 135 146
    • (1975) Synthesis , pp. 135-146
    • Lane, C.F.1
  • 39
    • 0001152361 scopus 로고
    • For a review of the Leuckart reaction, see: M.L. Moore R. Adams, Organic Reactions Vol. V 1948 John Wiely & Sons, Inc. New York 301 330
    • (1948) Organic Reactions , vol.5 , pp. 301-330
    • Moore, M.L.1
  • 44
    • 0001025601 scopus 로고
    • For examples, see: R.D. Bach J. Org. Chem. 33 1968 1647 1649
    • (1968) J. Org. Chem. , vol.33 , pp. 1647-1649
    • Bach, R.D.1
  • 53
    • 78649832129 scopus 로고    scopus 로고
    • Ref. 12b
    • Ref. 12b.
  • 56
    • 85004724143 scopus 로고
    • For a review on the use of ammonium formate in hydrogen transfer reactions, see: S. Ram, and R.E. Ehrenkaufer Synthesis 1988 91 95
    • (1988) Synthesis , pp. 91-95
    • Ram, S.1    Ehrenkaufer, R.E.2
  • 57
    • 78649890805 scopus 로고    scopus 로고
    • 3): δ 147.48, 146.34, 133.38, 121.81, 109.34, 107.82, 100.77, 60.40, 53.99, 23.37
    • 3): δ 147.48, 146.34, 133.38, 121.81, 109.34, 107.82, 100.77, 60.40, 53.99, 23.37.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.