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Volumn 13, Issue 13, 2011, Pages 3498-3501

Peptide/laccase cocatalyzed asymmetric α-oxyamination of aldehydes

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; LACCASE; OXIDE; PEPTIDE;

EID: 79959693358     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol2012956     Document Type: Article
Times cited : (37)

References (62)
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    • MacMillan et al. have developed the new class of reactions proceeding through SOMO activation with imidazolidinone catalysts and metal oxidizing reagents. For selected examples, see
    • MacMillan et al. have developed the new class of reactions proceeding through SOMO activation with imidazolidinone catalysts and metal oxidizing reagents. For selected examples, see: Beeson, T. D.; Mastracchio, A.; Hong, J.-B.; Ashton, K.; MacMillan, D. W. C. Science 2007, 316, 582
    • (2007) Science , vol.316 , pp. 582
    • Beeson, T.D.1    Mastracchio, A.2    Hong, J.-B.3    Ashton, K.4    MacMillan, D.W.C.5
  • 23
    • 77956551916 scopus 로고    scopus 로고
    • Maruoka et al. reported the α-oxyamination with TEMPO using a peroxide instead of a metal reagent.;;, For other examples of the α-oxyamination with TEMPO, see:; Chem. Lett. 2009, 38, 166
    • Maruoka et al. reported the α-oxyamination with TEMPO using a peroxide instead of a metal reagent. Kano, T.; Mii, H.; Maruoka, K. Angew. Chem., Int. Ed. 2010, 49, 6638 For other examples of the α-oxyamination with TEMPO, see: Koike, T.; Akita, M. Chem. Lett. 2009, 38, 166
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 6638
    • Kano, T.1    Mii, H.2    Maruoka, K.3    Koike, T.4    Akita, M.5
  • 31
    • 72949100542 scopus 로고    scopus 로고
    • reported the sequential reaction using an organocatalyst and alcohol dehydrogenase for the synthesis of chiral 1,3-diols. Baer, K.; Krauβer, M.; Burda, E.; Hummel, W.; Berkessel, A.; Gröger, H.
    • Gröger reported the sequential reaction using an organocatalyst and alcohol dehydrogenase for the synthesis of chiral 1,3-diols. Baer, K.; Krauβer, M.; Burda, E.; Hummel, W.; Berkessel, A.; Gröger, H. Angew. Chem., Int. Ed. 2009, 48, 9355.
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 9355
    • Gröger1
  • 32
    • 79959686358 scopus 로고    scopus 로고
    • n- means weight-average degree of polymerization.
    • n- means weight-average degree of polymerization.
  • 39
    • 77950392067 scopus 로고    scopus 로고
    • For recent selected examples of peptide-based asymmetric catalysts, see
    • For recent selected examples of peptide-based asymmetric catalysts, see: Fowler, B. S.; Mikochik, P. J.; Miller, S. J. J. Am. Chem. Soc. 2010, 132, 2870
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 2870
    • Fowler, B.S.1    Mikochik, P.J.2    Miller, S.J.3
  • 55
    • 19744364138 scopus 로고    scopus 로고
    • For examples for overoxidation of aldehydes to carboxylic acids, see: Marzorati, M.; Danieli, B.; Haltrich, D.; Riva, S.
    • For examples for overoxidation of aldehydes to carboxylic acids, see: Marzorati, M.; Danieli, B.; Haltrich, D.; Riva, S. Green Chem. 2005, 7, 310
    • (2005) Green Chem. , vol.7 , pp. 310
  • 62
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    • In entry 5 of Table 4, 0.05 mg (<0.002 mol %) of laccase was used for 0.05 mmol of the aldehyde. In other cases, 0.5 mg of laccase was used for the same amount of aldehydes. For experimental details, see Supporting Information.
    • In entry 5 of Table 4, 0.05 mg (<0.002 mol %) of laccase was used for 0.05 mmol of the aldehyde. In other cases, 0.5 mg of laccase was used for the same amount of aldehydes. For experimental details, see Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.