메뉴 건너뛰기




Volumn 7, Issue 19, 2015, Pages 3121-3124

Amination of ω-Functionalized Aliphatic Primary Alcohols by a Biocatalytic Oxidation-Transamination Cascade

Author keywords

alcohol oxidase; amination; biocatalysis; cascade; transaminase

Indexed keywords

ALCOHOLS; AMINES; ASPERGILLUS; BIOCATALYSTS; CASCADES (FLUID MECHANICS); MOLECULAR OXYGEN; OXIDATION;

EID: 84943353055     PISSN: 18673880     EISSN: 18673899     Source Type: Journal    
DOI: 10.1002/cctc.201500589     Document Type: Article
Times cited : (37)

References (34)
  • 1
    • 84926166921 scopus 로고    scopus 로고
    • (Eds.: S. Riva, W.-D. Fessner), Wiley-VCH, Weinheim
    • Cascade Biocatalysis (Eds.:, S. Riva, W.-D. Fessner,), Wiley-VCH, Weinheim, 2014;
    • (2014) Cascade Biocatalysis
  • 2
    • 84889432812 scopus 로고    scopus 로고
    • (Ed.: E. Garcia-Junceda) Wiley-VCH, Weinheim.
    • Multi-Step Enzyme Catalysis (Ed.:, E. Garcia-Junceda,) Wiley-VCH, Weinheim, 2008.
    • (2008) Multi-Step Enzyme Catalysis
  • 11
    • 78649716727 scopus 로고    scopus 로고
    • J. Keasling, Science 2010, 330, 1355-1358.
    • (2010) Science , vol.330 , pp. 1355-1358
    • Keasling, J.1
  • 12
    • 77949881748 scopus 로고    scopus 로고
    • The three most frequently occurring functional groups in chemical products are hydroxy (40%), carboxy (22%), and amino functionalities (16%), see:, in contrast, OH and CO2H groups largely dominate in renewable resources, see
    • The three most frequently occurring functional groups in chemical products are hydroxy (40%), carboxy (22%), and amino functionalities (16%), see:, S. M. Glueck, S. Gümüs, W. M. F. Fabian, K. Faber, Chem. Soc. Rev. 2010, 39, 313-328; in contrast, OH and CO2H groups largely dominate in renewable resources, see:
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 313-328
    • Glueck, S.M.1    Gümüs, S.2    Fabian, W.M.F.3    Faber, K.4
  • 19
    • 84863184863 scopus 로고    scopus 로고
    • Angew. Chem. 2012, 124, 3527-3530;
    • (2012) Angew. Chem. , vol.124 , pp. 3527-3530
  • 21
    • 81255209712 scopus 로고    scopus 로고
    • Angew. Chem. 2011, 123, 7741-7745.
    • (2011) Angew. Chem. , vol.123 , pp. 7741-7745
  • 30
    • 62949214480 scopus 로고    scopus 로고
    • Angew. Chem. 2008, 120, 9477-9480.
    • (2008) Angew. Chem. , vol.120 , pp. 9477-9480
  • 33
    • 84943366234 scopus 로고    scopus 로고
    • The same conversion of the model substrate 1-hexanol (3a) to the corresponding amine (3b) was obtained with ω-TA from Vibrio fluvialis.
    • The same conversion of the model substrate 1-hexanol (3a) to the corresponding amine (3b) was obtained with ω-TA from Vibrio fluvialis.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.