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Volumn 128, Issue 16, 2006, Pages 5358-5359

Free-radical version of the Strecker synthesis of α-aminoamides promoted by aqueous H2O2/TiCl3/HCONH 2 system

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; AMINO ACID DERIVATIVE; ANILINE DERIVATIVE; FORMAMIDE; FREE RADICAL; HYDROGEN PEROXIDE; TIN CHLORIDE;

EID: 33646449533     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja061092g     Document Type: Article
Times cited : (38)

References (39)
  • 1
    • 0028355337 scopus 로고
    • Selected reviews: (a) Duthaler, R. D. Tetrahedron 1994, 50, 1539-1650.
    • (1994) Tetrahedron , vol.50 , pp. 1539-1650
    • Duthaler, R.D.1
  • 4
    • 0041378065 scopus 로고    scopus 로고
    • (d) Groger, H. Chem. Rev. 2003, 103, 2795-2827.
    • (2003) Chem. Rev. , vol.103 , pp. 2795-2827
    • Groger, H.1
  • 9
    • 23944521388 scopus 로고    scopus 로고
    • and references quoted therein
    • (c) Jiang, B.; Huang, Z. G. Synthesis 2005, 2198-2204 and references quoted therein.
    • (2005) Synthesis , pp. 2198-2204
    • Jiang, B.1    Huang, Z.G.2
  • 15
    • 0035948184 scopus 로고    scopus 로고
    • For recent reviews on alkyl radical addition to C=N bonds, see: (a) Friestad, G. Tetrahedron 2001, 57, 5461-5496.
    • (2001) Tetrahedron , vol.57 , pp. 5461-5496
    • Friestad, G.1
  • 30
    • 33646453786 scopus 로고    scopus 로고
    • note
    • N-aryl arylglycines have been recently identified as a new class of human corticotropin releasing factor (CRF). See ref 3.
  • 31
    • 0032482080 scopus 로고    scopus 로고
    • A series of equilibria, not reported for simplicity, are involved in the formation of A. See: Azend, M.; Westermann, B.; Risch, N. Angew. Chem., Int. Ed. 1998, 37, 1044-1070.
    • (1998) Angew. Chem., Int. Ed. , vol.37 , pp. 1044-1070
    • Azend, M.1    Westermann, B.2    Risch, N.3
  • 32
    • 0000888302 scopus 로고
    • The carbamoyl radical has a clear-cut nucleophilic character, which permits amidation of protonated heteroaromatic bases. (a) Minisci, F.; Porta, O. Adv. Heterocycl. Chem. 1974, 16, 123-180.
    • (1974) Adv. Heterocycl. Chem. , vol.16 , pp. 123-180
    • Minisci, F.1    Porta, O.2
  • 33
    • 33646455332 scopus 로고    scopus 로고
    • Dicker, G., Ed.; Wiley-VCH Verlag GMBH: New York, Berlin
    • (b) Porta, O.; Minisci, F. Handbook of CH Transformations; Dicker, G., Ed.; Wiley-VCH Verlag GMBH: New York, Berlin, 2005; Vol. 1, pp 212-222.
    • (2005) Handbook of CH Transformations , vol.1 , pp. 212-222
    • Porta, O.1    Minisci, F.2
  • 38
    • 33646443067 scopus 로고    scopus 로고
    • EP 0002297, 1976
    • (b) Boesten, W. H. J. EP 0002297, 1976.
    • Boesten, W.H.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.