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Volumn 131, Issue 29, 2009, Pages 10003-10008

Catalytic transamidation reactions compatible with tertiary amide metathesis under ambient conditions

Author keywords

[No Author keywords available]

Indexed keywords

AMBIENT CONDITIONS; AMIDO COMPLEXES; CARBOXAMIDES; CATALYTIC ACTIVITY; CONTROLLED REACTIONS; EFFICIENT CATALYSTS; NITROGEN BONDS; ROOM TEMPERATURE; SECONDARY AMINES; TERTIARY AMIDES; TRANSAMIDATION; TRANSAMIDATION REACTION;

EID: 67651208251     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja8094262     Document Type: Article
Times cited : (187)

References (39)
  • 1
    • 0032820242 scopus 로고    scopus 로고
    • For recent reviews of dynamic covalent chemistry: a
    • For recent reviews of dynamic covalent chemistry: (a) Lehn, J.-M. Chem. Eur. J. 1999, 5, 2455-2463.
    • (1999) Chem. Eur. J , vol.5 , pp. 2455-2463
    • Lehn, J.-M.1
  • 5
    • 0343372213 scopus 로고    scopus 로고
    • Transamidation at very high temperatures (>250°C), typically with polyamides, has been reported: (a) Smith, M. E.; Adkins, H. J. Am. Chem. Soc. 1938, 60, 657-663.
    • Transamidation at very high temperatures (>250°C), typically with polyamides, has been reported: (a) Smith, M. E.; Adkins, H. J. Am. Chem. Soc. 1938, 60, 657-663.
  • 9
    • 67651230110 scopus 로고
    • U.S. Patent 5,302,756
    • (e) McKinney, R. J. U.S. Patent 5,302,756, 1994.
    • (1994)
    • McKinney, R.J.1
  • 10
    • 67651228944 scopus 로고
    • U.S. Patent 5,395,974
    • (f) McKinney, R. J. U.S. Patent 5,395,974, 1995.
    • (1995)
    • McKinney, R.J.1
  • 11
    • 0026042519 scopus 로고
    • For enzymatic approaches to secondary-amide exchange reactions, see: a
    • For enzymatic approaches to secondary-amide exchange reactions, see: (a) Gotor, V.; Brieva, R.; González, C.; Rebolledo, F. Tetrahedron 1991, 47, 9207-9214.
    • (1991) Tetrahedron , vol.47 , pp. 9207-9214
    • Gotor, V.1    Brieva, R.2    González, C.3    Rebolledo, F.4
  • 14
    • 0005827055 scopus 로고    scopus 로고
    • Precedents for transamidation under synthetically practical conditions are typically limited to intramolecular reactions or require a stoichiometric reagent: (a) Galat, A, Elion, G. J. Am. Chem. Soc. 1943, 65, 1566-1567
    • Precedents for transamidation under synthetically practical conditions are typically limited to intramolecular reactions or require a stoichiometric reagent: (a) Galat, A.; Elion, G. J. Am. Chem. Soc. 1943, 65, 1566-1567.
  • 29
    • 33846544889 scopus 로고    scopus 로고
    • Secondary amide metathesis can achieved by imide-catalyzed transacylation (i.e., without the involvment of amine-amide exchange steps), but this process requires high temperatures: Bell, C. M.; Kissounko, D. A.; Gellman, S. H.; Stahl, S. S. Angew. Chem., Int. Ed. 2007, 46, 761-763.
    • Secondary amide metathesis can achieved by imide-catalyzed transacylation (i.e., without the involvment of amine-amide exchange steps), but this process requires high temperatures: Bell, C. M.; Kissounko, D. A.; Gellman, S. H.; Stahl, S. S. Angew. Chem., Int. Ed. 2007, 46, 761-763.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.