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Volumn , Issue 4, 2006, Pages 533-538

Design and synthesis of a new generation of 'NH'-Ni(II) complexes of glycine Schiff bases and their unprecedented C-H vs. N-H chemoselectivity in alkyl halide alkylations and Michael addition reactions

Author keywords

Amino acids; Chemoselectivity; Chiral auxiliary; Nickel; Schiff base

Indexed keywords

ACETAMIDE DERIVATIVE; CARBON; GLYCINE; HYDROGEN; N (2 BENZOYLPHENYL) 2 AMINOACETAMIDE DERIVATIVE; NICKEL COMPLEX; NITROGEN; SCHIFF BASE; UNCLASSIFIED DRUG;

EID: 33644991932     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-926252     Document Type: Article
Times cited : (13)

References (47)
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    • (2004) Tetrahedron Lett. , vol.45 , pp. 9159
    • Taylor, S.M.1    Yamada, T.2    Ueki, H.3    Soloshonok, V.A.4
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    • For recent applications of Hünig's base for the efficient synthesis of tertiary amines, see: Moore, J. L.; Taylor, S. M.; Soloshonok, V. A. ARKIVOC 2005, (vi), 287.
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    • Moore, J.L.1    Taylor, S.M.2    Soloshonok, V.A.3
  • 30
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    • (a) Although Professor Hegedus does mention that the complexation of a secondary amino group to Ni(II) was not sufficient to create the desired chemoselectivity of O-H over N-H acylation, he does introduce the idea of using it as a form of protection. See: Hegedus, L. S.; Greenberg, M. M.; Wendling, J. J.; Bullock, J. P. J. Org. Chem. 2003, 68, 4179.
    • (2003) J. Org. Chem. , vol.68 , pp. 4179
    • Hegedus, L.S.1    Greenberg, M.M.2    Wendling, J.J.3    Bullock, J.P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.