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Volumn 129, Issue 2, 2007, Pages 282-283

Enantioselective synthesis of α-tertiary hydroxyaldehydes by palladium-catalyzed asymmetric allylic alkylation of enolates

Author keywords

[No Author keywords available]

Indexed keywords

ALLYL COMPOUND; ENOLATE; HYDROXYALDEHYDE; HYDROXYALDEHYDE DERIVATIVE; KETONE DERIVATIVE; OXYBUTYNIN; PALLADIUM; UNCLASSIFIED DRUG;

EID: 33846192045     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja067342a     Document Type: Article
Times cited : (98)

References (27)
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    • Jacobsen, E. N, Pfaltz, A, Yamamoto, H, Eds, Springer: Berlin
    • (a) Hughes, D. L. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, 1999; Vol. 3, p 1273.
    • (1999) Comprehensive Asymmetric Catalysis , vol.3 , pp. 1273
    • Hughes, D.L.1
  • 13
    • 3242806955 scopus 로고    scopus 로고
    • Enantioseletive aldol reactions of α-oxyaldehydes catalyzed by organocatalysts have been reported. See
    • Enantioseletive aldol reactions of α-oxyaldehydes catalyzed by organocatalysts have been reported. See: Northrup, A. B.; Mangion, I. K.; Hettche, F.; MacMillian, D. W. C. Angew. Chem., Int. Ed. 2004, 43, 2152.
    • (2004) Angew. Chem., Int. Ed , vol.43 , pp. 2152
    • Northrup, A.B.1    Mangion, I.K.2    Hettche, F.3    MacMillian, D.W.C.4
  • 16
    • 9344253873 scopus 로고    scopus 로고
    • Similar results were reported independently by Stoltz et al. using t-Bu-PHOX ligands. See
    • (c) Similar results were reported independently by Stoltz et al. using t-Bu-PHOX ligands. See: Behenna, D. C.; Stoltz, B. M. J. Am. Chem. Soc. 2004, 126, 15044.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 15044
    • Behenna, D.C.1    Stoltz, B.M.2
  • 17
    • 33846204606 scopus 로고    scopus 로고
    • See Supporting Information for the examples of the synthesis of siloxy enol carbonates
    • See Supporting Information for the examples of the synthesis of siloxy enol carbonates.
  • 19
    • 27644456225 scopus 로고    scopus 로고
    • For the synthesis of (S)-oxybutynin see: (b) Tokuda, O.; Kano, T.; Gao, W. G.; Ikemoto, T.; Maruoka, K. Org. Lett. 2005, 7, 5103.
    • For the synthesis of (S)-oxybutynin see: (b) Tokuda, O.; Kano, T.; Gao, W. G.; Ikemoto, T.; Maruoka, K. Org. Lett. 2005, 7, 5103.
  • 24
    • 0028955943 scopus 로고    scopus 로고
    • 3)). Agami, C.; Couty, F.; Lequesne, C. Tetrahedron 1995, 51, 4043.
    • 3)). Agami, C.; Couty, F.; Lequesne, C. Tetrahedron 1995, 51, 4043.
  • 26
    • 0001501419 scopus 로고    scopus 로고
    • 26 = +124.7 (c 0.635, benzene)). Soai, K.; Ishizaki, M. J. Org. Chem. 1986, 51, 3290.
    • 26 = +124.7 (c 0.635, benzene)). Soai, K.; Ishizaki, M. J. Org. Chem. 1986, 51, 3290.
  • 27
    • 0029932015 scopus 로고    scopus 로고
    • 3)). Compain, P.; Goré, J.; Vatèle, J. M. Tetrahedron 1996, 52, 6647.
    • 3)). Compain, P.; Goré, J.; Vatèle, J. M. Tetrahedron 1996, 52, 6647.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.