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Volumn 129, Issue 2, 2007, Pages 276-277

Cu(I) Tol-BINAP-catalyzed enantioselective Michael reactions of Grignard reagents and unsaturated esters

Author keywords

[No Author keywords available]

Indexed keywords

COPPER; ESTER DERIVATIVE; GRIGNARD REAGENT; REAGENT; UNCLASSIFIED DRUG;

EID: 33846250465     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0666046     Document Type: Article
Times cited : (103)

References (17)
  • 2
    • 33846209898 scopus 로고
    • Conjugate Addition Reactions in Organic Synthesis; Tetrahedron Organic Chemistry
    • Pergamon: Oxford
    • (b) Perlmutter, P. Conjugate Addition Reactions in Organic Synthesis; Tetrahedron Organic Chemistry, Series 9; Pergamon: Oxford, 1992.
    • (1992) Series , vol.9
    • Perlmutter, P.1
  • 11
    • 0034703410 scopus 로고    scopus 로고
    • Besides Feringa group's work (ref 3c), only a Rh-catalyzed asymmetric conjugate addition of aryl boron reagents to α,β-unsaturated esters has been reported. (a) Sakuma, S.; Sakai, M.; Itooka, R.; Miyaura, N. J. Org. Chem. 2000, 65, 5951-5955.
    • Besides Feringa group's work (ref 3c), only a Rh-catalyzed asymmetric conjugate addition of aryl boron reagents to α,β-unsaturated esters has been reported. (a) Sakuma, S.; Sakai, M.; Itooka, R.; Miyaura, N. J. Org. Chem. 2000, 65, 5951-5955.
  • 15
    • 33846196960 scopus 로고    scopus 로고
    • 2, and THF gave the product in lower ee (< 80% ee).
    • 2, and THF gave the product in lower ee (< 80% ee).
  • 16
    • 33846233283 scopus 로고    scopus 로고
    • See Supporting Information
    • See Supporting Information.
  • 17
    • 33846229126 scopus 로고    scopus 로고
    • 3c the desired products were obtained with improved yields and enantioselectivities. (Diagram presented)
    • 3c the desired products were obtained with improved yields and enantioselectivities. (Diagram presented)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.