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Volumn 60, Issue 35, 2004, Pages 7543-7552

Asymmetric reactions of axially chiral amides: Use of removable ortho-substituents in radical cyclizations of o-iodoacrylanilides and N-allyl-N-o-iodoacrylamides

Author keywords

Asymmetric radical reactions; Axially chiral amides

Indexed keywords

ACRYLAMIDE DERIVATIVE; AMIDE; ANILIDE; IODINE DERIVATIVE; NITROGEN DERIVATIVE; RADICAL;

EID: 3843117909     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.05.116     Document Type: Article
Times cited : (47)

References (36)
  • 7
    • 3843110770 scopus 로고    scopus 로고
    • Tetrahedron symposium-in-print on asymmetric reactions of axially chiral amides
    • (c) See also the recent Tetrahedron Symposium-in-Print on Asymmetric Reactions of Axially Chiral Amides, Clayden, J., Ed., Tetrahedron 2004, 60(20), 4325-4558.
    • (2004) Tetrahedron , vol.60 , Issue.20 , pp. 4325-4558
    • Clayden, J.1
  • 17
    • 0041878683 scopus 로고    scopus 로고
    • For review on enantioselective radical reactions:
    • For review on enantioselective radical reactions: Sibi M.P., Manyem S., Zimmerman J. Chem. Rev. 103:2003;3263-3296
    • (2003) Chem. Rev. , vol.103 , pp. 3263-3296
    • Sibi, M.P.1    Manyem, S.2    Zimmerman, J.3
  • 20
    • 0038392407 scopus 로고    scopus 로고
    • For review on oxindole alkaloids see:
    • For review on oxindole alkaloids see: Marti C., Carreira E. Eur. J. Org. Chem. 2003;2209-2219
    • (2003) Eur. J. Org. Chem. , pp. 2209-2219
    • Marti, C.1    Carreira, E.2
  • 28
    • 3843080298 scopus 로고    scopus 로고
    • Traces of uncyclized, reduced compounds (between 1-5%) were also isolated by chromatography on silica gel
    • Traces of uncyclized, reduced compounds (between 1-5%) were also isolated by chromatography on silica gel
  • 30
    • 0000707331 scopus 로고
    • Rate constant measurements show that aryl iodides are about 400 times more reactive than aryl bromides towards tributyltin radical
    • Rate constant measurements show that aryl iodides are about 400 times more reactive than aryl bromides towards tributyltin radical Curran D.P., Jasperse C.P., Totleben M.J. J. Org. Chem. 56:1991;7169-7172
    • (1991) J. Org. Chem. , vol.56 , pp. 7169-7172
    • Curran, D.P.1    Jasperse, C.P.2    Totleben, M.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.