메뉴 건너뛰기




Volumn 5, Issue 8, 2015, Pages 4708-4712

Development of DNA Metalloenzymes Using a Rational Design Approach and Application in the Asymmetric Diels-Alder Reaction

Author keywords

asymmetric catalysis; Cu(II) ion; Diels Alder reaction; DNA; enantiomeric preference; ligand freedom; metalloenzyme

Indexed keywords

CATALYSIS; CHEMICAL REACTIONS; ENANTIOMERS; ENZYMES; LIGANDS; METALS; NUCLEIC ACIDS;

EID: 84938709492     PISSN: 21555435     EISSN: None     Source Type: Journal    
DOI: 10.1021/acscatal.5b01046     Document Type: Article
Times cited : (44)

References (43)
  • 4
    • 33748634910 scopus 로고    scopus 로고
    • Lu, Y. Angew. Chem., Int. Ed. 2006, 45, 5588-5601 10.1002/anie.200600168
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 5588-5601
    • Lu, Y.1
  • 8
    • 33846524196 scopus 로고    scopus 로고
    • Roelfes, G. Mol. BioSyst. 2007, 3, 126-135 10.1039/B614527B
    • (2007) Mol. BioSyst. , vol.3 , pp. 126-135
    • Roelfes, G.1
  • 12
    • 84870170094 scopus 로고    scopus 로고
    • Park, S.; Sugiyama, H. Molecules 2012, 17, 12792-12803 10.3390/molecules171112792
    • (2012) Molecules , vol.17 , pp. 12792-12803
    • Park, S.1    Sugiyama, H.2
  • 35
    • 84938732841 scopus 로고    scopus 로고
    • note
    • Complementary strands of ODN6 containing natural bases (A, T, and G) were also examined to investigate the counter base effect. The DNA metalloenzymes by the combination of triethylene glycol and a counter base A, T, or G afforded lower enantioselectivities of product compared with a counter base C (entries 1-3 in Table S2).
  • 36
    • 84938732842 scopus 로고    scopus 로고
    • note
    • In the case of dienophile including a p-nitro group on the phenyl ring, a decrease in enantioselectivity was observed using a Cu(II)-DNA-triethylene glycol conjugate (99% conversion, endo/exo = 18/1, -59% ee).
  • 43
    • 84938732843 scopus 로고    scopus 로고
    • note
    • The control experiment using a Cu(II)-dmbpy/ODN6/ODN15 system afforded the Diels-Alder product with -87% ee, endo/exo ratio of 36:1 and 97% conversion.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.