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Volumn 69, Issue 9, 2011, Pages 985-993

Catalytic enantioselective synthesis of novel atropisomeric compounds having an N-C chiral axis and their application to asymmetric reaction

Author keywords

Anilide; Aromatic amination; Atropisomerism; Catalytic enantioselective reaction; Chiral phosphine; Hydroaminocyclization; Indole; Lactam; N c chiral axis; Palladium

Indexed keywords

ANILIDE; ATROPISOMERISM; CHIRAL PHOSPHINE; ENANTIOSELECTIVE REACTIONS; HYDROAMINOCYCLIZATION; INDOLE; LACTAM; N-C CHIRAL AXIS;

EID: 81155137588     PISSN: 00379980     EISSN: None     Source Type: Journal    
DOI: 10.5059/yukigoseikyokaishi.69.985     Document Type: Article
Times cited : (15)

References (66)
  • 6
    • 81155145266 scopus 로고    scopus 로고
    • L. H. Pa, Chem. Rev., 98, 2405(1998):
    • (1998) Chem. Rev. , vol.98 , pp. 2405
    • Pa, L.H.1
  • 9
    • 81155149375 scopus 로고
    • Typical examples of atropisomeric compounds having an N-C chiral axis
    • Typical examples of atropisomeric compounds having an N-C chiral axis: (a)L. H. Bock. R. Adams, J. Am. Chem. Soc., 53, 374(1931);
    • (1931) J. Am. Chem. Soc. , vol.53 , pp. 374
    • Bock, L.H.1    Adams, R.2
  • 21
    • 3843110770 scopus 로고    scopus 로고
    • Tetrahedron Symposiumin-print on Axially Chiral Amides (Atropisomerism)
    • Tetrahedron Symposiumin-print on Axially Chiral Amides (Atropisomerism), J. Claydea Ed., Tetrahedron, 60, 4325(2004);
    • (2004) Tetrahedron , vol.60 , pp. 4325
    • Claydea, J.1
  • 32
    • 0002795445 scopus 로고
    • For reviews on catalytic asymmetric allylation with a chiral π-allyl-Pd complex: ed. by I. Ojima VCH Publishers. New York
    • For reviews on catalytic asymmetric allylation with a chiral π-allyl-Pd complex: (a)T. Hayashi, "Catalytic Asymmetric Synthesis" ed. by I. Ojima VCH Publishers. New York, 1994, p 325;
    • (1994) Catalytic Asymmetric Synthesis , pp. 325
    • Hayashi, T.1
  • 46
    • 0001203745 scopus 로고
    • The C = C part of the amide enolates is well known to prefer the Z-form
    • The C = C part of the amide enolates is well known to prefer the Z-form: (a) D. A. Evans, J. M. Takacs, Tetrahedron Lett., 21. 4233(1980);
    • (1980) Tetrahedron Lett. , vol.21 , pp. 4233
    • Evans, D.A.1    Takacs, J.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.