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Volumn 128, Issue 3, 2006, Pages 734-735

Organocatalytic direct asymmetric aldol reactions in water

Author keywords

[No Author keywords available]

Indexed keywords

ORGANIC COMPOUND; WATER;

EID: 31444456557     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0573312     Document Type: Article
Times cited : (678)

References (23)
  • 2
    • 0036105107 scopus 로고    scopus 로고
    • See also references therein
    • (b) Kobayashi, S.; Manabe, K. Acc. Chem. Res. 2002, 35, 209-217. See also references therein.
    • (2002) Acc. Chem. Res. , vol.35 , pp. 209-217
    • Kobayashi, S.1    Manabe, K.2
  • 18
    • 0037037912 scopus 로고    scopus 로고
    • Diamine 8a/acid bifunctional catalysts catalyzed aldol reactions with high enantioselectivities in conventional organic solvents, (a) Nakadai, M.; Saito, S.; Yamamoto, H. Tetrahedron 2002, 58, 8167-8177.
    • (2002) Tetrahedron , vol.58 , pp. 8167-8177
    • Nakadai, M.1    Saito, S.2    Yamamoto, H.3
  • 21
    • 31444436439 scopus 로고    scopus 로고
    • note
    • The diamine 8b/TFA-catalyzed reaction in water: To a mixture of diamine 8b (0.05 mmol) in water (1.0 mL) trifluoroacetic acid (0.05 mmol) was added at 25 °C under air. The reaction mixture was stirred for 3 min in a closed system, and ketone (1.0 mmol) and aldehyde (0.5 mmol) were added. The reaction mixture was vigorously stirred for the indicated time. Removal of water by centrifugal separation and purification of crude product by column chromatography afforded the aldol product.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.