메뉴 건너뛰기




Volumn 64, Issue 14, 1999, Pages 5017-5023

Palladium(II)-catalyzed asymmetric 1,3-dipolar cycloaddition of nitrones to 3-alkenoyl-1,3-oxazolidin-2-ones

Author keywords

[No Author keywords available]

Indexed keywords

ALKENYL GROUP; CARBOXYLIC ACID DERIVATIVE; LIGAND; OXAZOLIDINE DERIVATIVE; PALLADIUM; PHOSPHINE DERIVATIVE; RUTHENIUM COMPLEX;

EID: 0032997310     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo981483g     Document Type: Article
Times cited : (95)

References (55)
  • 19
    • 3242881202 scopus 로고    scopus 로고
    • The review of asymmetric 1,3-dipolar cycloaddition: (a) Gothelf, K. V.; Jørgensen, K. A. Acta Chem. Scand. 1996, 50, 652-660. (b) Frederickson, M. Tetrahedron 1997, 53, 403-425. (c) Gothelf, K. V.; Jørgensen, K. A. Chem. Rev. 1998, 98, 863-909.
    • (1996) Acta Chem. Scand. , vol.50 , pp. 652-660
    • Gothelf, K.V.1    Jørgensen, K.A.2
  • 20
    • 0031012571 scopus 로고    scopus 로고
    • The review of asymmetric 1,3-dipolar cycloaddition: (a) Gothelf, K. V.; Jørgensen, K. A. Acta Chem. Scand. 1996, 50, 652-660. (b) Frederickson, M. Tetrahedron 1997, 53, 403-425. (c) Gothelf, K. V.; Jørgensen, K. A. Chem. Rev. 1998, 98, 863-909.
    • (1997) Tetrahedron , vol.53 , pp. 403-425
    • Frederickson, M.1
  • 21
    • 11544346529 scopus 로고    scopus 로고
    • The review of asymmetric 1,3-dipolar cycloaddition: (a) Gothelf, K. V.; Jørgensen, K. A. Acta Chem. Scand. 1996, 50, 652-660. (b) Frederickson, M. Tetrahedron 1997, 53, 403-425. (c) Gothelf, K. V.; Jørgensen, K. A. Chem. Rev. 1998, 98, 863-909.
    • (1998) Chem. Rev. , vol.98 , pp. 863-909
    • Gothelf, K.V.1    Jørgensen, K.A.2
  • 37
    • 0003544583 scopus 로고
    • VCH: New York
    • For the chiral phosphine ligands used and their abbreviations, see: (a) Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH: New York, 1993. (b) Chiral Auxiliaries and Ligands in Asymmetric Synthesis; Seyden-Penne, J., Ed.; Wiley: New York, 1995.
    • (1993) Catalytic Asymmetric Synthesis
    • Ojima, I.1
  • 40
    • 4244033876 scopus 로고
    • The review of catalytic asymmetric Diels-Alder reactions: (a) Kagan, H. B.; Riant, O. Chem. Rev. 1992, 92, 1007-1019. (b) Dias, L. C. J. Braz. Chem. Soc. 1997, 8, 289-332.
    • (1992) Chem. Rev. , vol.92 , pp. 1007-1019
    • Kagan, H.B.1    Riant, O.2
  • 41
    • 0031371093 scopus 로고    scopus 로고
    • The review of catalytic asymmetric Diels-Alder reactions: (a) Kagan, H. B.; Riant, O. Chem. Rev. 1992, 92, 1007-1019. (b) Dias, L. C. J. Braz. Chem. Soc. 1997, 8, 289-332.
    • (1997) J. Braz. Chem. Soc. , vol.8 , pp. 289-332
    • Dias, L.C.1
  • 45
    • 0345297974 scopus 로고    scopus 로고
    • note
    • D = +5.5 (51% ee), and the absolute configuration of the isoxazolidine ring of (+)-endo-3b was assigned as 3S,4R,5S in the literature (see ref 6c).
  • 46
    • 0344434937 scopus 로고    scopus 로고
    • note
    • D = -13.1 (75% ee), and the absolute configuration of the isoxazolidine ring of (-)-endo-3c was assigned as 3S,4R,5S in the literature (see ref 9a).
  • 55
    • 0344434934 scopus 로고    scopus 로고
    • note
    • 1H NMR spectra by coupling constants as well as NOE analysis (see ref 12).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.