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Volumn 2003, Issue 7, 2003, Pages 49-58

Enantioselective intramolecular 1,3-dipolar cycloadditions ofdiazocarbonyl-derived oxidopyryliums

Author keywords

Asymmetric catalysis; Cycloadditions; Diazo compounds; Oxidopyryliums; Rhodium

Indexed keywords

(BUT 3 ENYL)METHYL 2 [(BUT 3 ENYL) 2 PHENYLCARBOXYLATE]MALONATE; 9,10 BENZO 2,11 DIOXATRICYCLO[5.3.1.0 1,5 ]UNDECAN 8 ONE; 9,10 BENZO 7 CARBOMETHOXY 2,11 DIOXATRICYCLO[5.3.1.0 1,5 ]UNDECAN 8 ONE; ACID ANHYDRIDE; CARBONYL DERIVATIVE; DIAZOCARBONYL DERIVATIVE; HETEROCYCLIC COMPOUND; METHYL 4 HYDROXY 1 OXO 1H ISOCHROMENE 3 CARBOXYLATE; OXIDOPYRYLIUM DERIVATIVE; PHTHALIC ANHYDRIDE; UNCLASSIFIED DRUG;

EID: 0042787617     PISSN: 14246376     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (11)

References (23)
  • 14
    • 0037243592 scopus 로고    scopus 로고
    • Hodgson, D. M.; Stupple, P. A.; Pierard, F. Y. T. M.; Labande, A. H.; Johnstone, C. Chem. Eur. J. 2001, 7, 4465. See also: Hodgson, D. M.; Labande, A. H.; Pierard, F. Y. T. M. Synlett 2003, 59.
    • (2003) Synlett , pp. 59
    • Hodgson, D.M.1    Labande, A.H.2    Pierard, F.Y.T.M.3
  • 15
    • 0026463995 scopus 로고
    • Pirrung, M. C.; Zhang, J. Tetrahedron Lett. 1992, 33, 5987. For a related chiral Rh(II) phosphate catalyst reported contemporaneously by McKervey, see: McCarthy, N.; McKervey, M. A.; Ye, T.; McCann, M.; Murphy, E.; Doyle, M. P. Tetrahedron Lett. 1992, 33, 5983.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 5987
    • Pirrung, M.C.1    Zhang, J.2
  • 18
    • 0034730008 scopus 로고    scopus 로고
    • up to 93% ee using DMAD
    • Kitagaki, S.; Yasugahira, M.; Anada, M.; Nakajima, M.; Hashimoto, S. Tetrahedron Lett. 2000, 41, 5931 (up to 93% ee using DMAD); Suga, H.; Inoue, K.; Inoue, S.; Kakehi, A. J. Am. Chem. Soc. 2002, 124, 14836 (up to 98% ee using an 3-acryloyl-2-oxazolidinone with a chiral Lewis acid-Rh catalyst combination).
    • (2000) Tetrahedron Lett. , vol.41 , pp. 5931
    • Kitagaki, S.1    Yasugahira, M.2    Anada, M.3    Nakajima, M.4    Hashimoto, S.5
  • 19
    • 0037132621 scopus 로고    scopus 로고
    • up to 98% ee using an 3-acryloyl-2-oxazolidinone with a chiral Lewis acid-Rh catalyst combination
    • Kitagaki, S.; Yasugahira, M.; Anada, M.; Nakajima, M.; Hashimoto, S. Tetrahedron Lett. 2000, 41, 5931 (up to 93% ee using DMAD); Suga, H.; Inoue, K.; Inoue, S.; Kakehi, A. J. Am. Chem. Soc. 2002, 124, 14836 (up to 98% ee using an 3-acryloyl-2-oxazolidinone with a chiral Lewis acid-Rh catalyst combination).
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 14836
    • Suga, H.1    Inoue, K.2    Inoue, S.3    Kakehi, A.4
  • 21
    • 3242719230 scopus 로고    scopus 로고
    • note
    • No satisfactory analytical method could be found for resolving the cycloadduct from corresponding ethyl ester.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.