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Volumn 127, Issue 20, 2005, Pages 7284-7285

Catalytic enantioselective thioester aldol reactions that are compatible with protic functional groups

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; BENZALDEHYDE; COPPER; NICKEL; OXAZOLINE DERIVATIVE; THIOESTER;

EID: 19744363827     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja051759j     Document Type: Article
Times cited : (159)

References (23)
  • 2
    • 0000699983 scopus 로고    scopus 로고
    • Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer-Verlag: Berlin
    • For a review of catalytic, enantioselective Mukaiyama aldol reactions with silyl ketene acetals, see: (b) Carreira, E. M. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer-Verlag: Berlin, 1999; Vol. 3, pp 997-1065.
    • (1999) Comprehensive Asymmetric Catalysis , vol.3 , pp. 997-1065
    • Carreira, E.M.1
  • 4
    • 2342504471 scopus 로고    scopus 로고
    • For other catalytic enantioselective aldol reactions with esters or their derivatives involving in situ generation of the nucleophile, see:. (a) Zhu, C.; Shen, X.; Nelson, S. G. J Am. Chem. Soc. 2004, 126, 5352-5.353..
    • (2004) J Am. Chem. Soc. , vol.126 , pp. 5352-5353
    • Zhu, C.1    Shen, X.2    Nelson, S.G.3
  • 11
    • 19744380223 scopus 로고    scopus 로고
    • note
    • MeMAHT. (1) was prepared in 12 g batches in one step from commercially available starting materials, in 94% yield, and without chromatography following crystallization. (see Supporting Information). 1 is a colorless solid that can be stored on the benchtop for at least 2 months without loss of activity in the aldol reaction.
  • 19
    • 2442510937 scopus 로고    scopus 로고
    • and references therein
    • (c) Yu, Y.; Liebeskind, L. S. J. Org. Chem. 2004, 69, 3554-3557 and references therein.
    • (2004) J. Org. Chem. , vol.69 , pp. 3554-3557
    • Yu, Y.1    Liebeskind, L.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.