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Volumn 75, Issue 14, 2010, Pages 4872-4875

Organocatalytic enantioselective hydroxymethylation of oxindoles with paraformaldehyde as C1 unit

Author keywords

[No Author keywords available]

Indexed keywords

BIFUNCTIONAL; ENANTIOSELECTIVE; HIGH ENANTIOSELECTIVITY; HYDROXYMETHYLATION; MILD REACTION CONDITIONS; ORGANOCATALYSTS; ORGANOCATALYTIC; OXINDOLES; PARAFORMALDEHYDES; QUATERNARY CARBON; STERICALLY CONGESTED; TERTIARY AMINE;

EID: 77954543828     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo100769n     Document Type: Article
Times cited : (107)

References (84)
  • 1
  • 6
    • 0037191618 scopus 로고    scopus 로고
    • For selected examples, see
    • For selected examples, see: Wearing, X. Z.; Cook, J. M. Org. Lett. 2002, 4, 4237
    • (2002) Org. Lett. , vol.4 , pp. 4237
    • Wearing, X.Z.1    Cook, J.M.2
  • 12
    • 22944468852 scopus 로고    scopus 로고
    • For the synthesis of 3,3-disubstituted oxindoles via transition-metal- catalyzed asymmetric reactions, see
    • For the synthesis of 3,3-disubstituted oxindoles via transition-metal- catalyzed asymmetric reactions, see: Hamashima, Y.; Suzuki, T.; Takano, H.; Shimura, Y.; Sodeoka, M. J. Am. Chem. Soc. 2005, 127, 10164
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 10164
    • Hamashima, Y.1    Suzuki, T.2    Takano, H.3    Shimura, Y.4    Sodeoka, M.5
  • 23
    • 0042819678 scopus 로고    scopus 로고
    • For the synthesis of 3,3-disubstituted oxindoles via organocatalytic asymmetric reactions, see
    • For the synthesis of 3,3-disubstituted oxindoles via organocatalytic asymmetric reactions, see: Hills, I. D.; Fu, G. C. Angew. Chem., Int. Ed. 2003, 42, 3921
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 3921
    • Hills, I.D.1    Fu, G.C.2
  • 45
    • 0002062967 scopus 로고    scopus 로고
    • For direct aldol reactions involving formaldehyde with transition-metal catalysts, see
    • For direct aldol reactions involving formaldehyde with transition-metal catalysts, see: Kuwano, R.; Miyazaki, H.; Ito, Y. Chem. Commun. 1998, 71
    • (1998) Chem. Commun. , pp. 71
    • Kuwano, R.1    Miyazaki, H.2    Ito, Y.3
  • 54
    • 4644267501 scopus 로고    scopus 로고
    • For some selected examples of indirect asymmetric aldol reaction of formaldehyde with silyl enolates, see
    • For some selected examples of indirect asymmetric aldol reaction of formaldehyde with silyl enolates, see: Ozawa, N.; Wadamoto, M.; Ishihara, K.; Yamamoto, H. Synlett 2003, 2219
    • (2003) Synlett , pp. 2219
    • Ozawa, N.1    Wadamoto, M.2    Ishihara, K.3    Yamamoto, H.4
  • 58
    • 50249134990 scopus 로고    scopus 로고
    • For selected reviews on organocatalytic asymmetric reactions, see
    • For selected reviews on organocatalytic asymmetric reactions, see: Denmark, S. E.; Beutner, G. L. Angew. Chem., Int. Ed. 2008, 47, 1560
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 1560
    • Denmark, S.E.1    Beutner, G.L.2
  • 62
    • 29844448114 scopus 로고    scopus 로고
    • For selected reviews of bifunctional urea and thiourea catalysts, see
    • For selected reviews of bifunctional urea and thiourea catalysts, see: Takemoto, Y. Org. Biomol. Chem. 2005, 3, 4299
    • (2005) Org. Biomol. Chem. , vol.3 , pp. 4299
    • Takemoto, Y.1
  • 75
    • 0142072631 scopus 로고    scopus 로고
    • For the synthesis of chiral bifunctional thiourea-tertiary amine catalysts, see
    • For the synthesis of chiral bifunctional thiourea-tertiary amine catalysts, see: Okino, T.; Hoashi, Y.; Takemoto, Y. J. Am. Chem. Soc. 2003, 125, 12672
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 12672
    • Okino, T.1    Hoashi, Y.2    Takemoto, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.