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Volumn 48, Issue 30, 2009, Pages 5521-5525

Asymmetric self- and cross-aldol reactions of glycolaldehyde catalyzed by d-fructose-6-phosphate aldolase

Author keywords

Aldol reaction; Aldolases; Aldoses; Enzyme catalysis; Glycolaldehydes

Indexed keywords

ALDOL REACTION; ALDOLASES; ALDOSES; ENZYME CATALYSIS; GLYCOLALDEHYDES;

EID: 70349931172     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200902065     Document Type: Article
Times cited : (117)

References (48)
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    • Angew Chem. Int. Ed. 2004, 43, 2152-2154.
    • (2004) Angew Chem. Int. Ed , vol.43 , pp. 2152-2154
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    • 34250821619 scopus 로고    scopus 로고
    • Angew Chem. Int. Ed. 2007, 46, 1738-1740.
    • (2007) Angew Chem. Int. Ed , vol.46 , pp. 1738-1740
  • 20
    • 70349939897 scopus 로고    scopus 로고
    • The control of the donor and acceptor aldehyde depended upon their intrinsic reactivity: the donors always possess an accessible enolizable α proton i.e. kinetically favored, whereas the acceptors are sterically hindered, β, β-disubstituted, or kinetically inaccessible α, α-disubtituted aldehydes
    • The control of the donor and acceptor aldehyde depended upon their intrinsic reactivity: the donors always possess an accessible enolizable α proton (i.e. kinetically favored), whereas the acceptors are sterically hindered, β, β-disubstituted, or kinetically inaccessible α, α-disubtituted aldehydes.
  • 33
    • 70349963202 scopus 로고    scopus 로고
    • 27-30]
    • 27-30]
  • 34
    • 70349927365 scopus 로고    scopus 로고
    • 13CNMR spectroscopy, only the syn diasteromer was observed.
    • 13CNMR spectroscopy, only the syn diasteromer was observed.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.