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Volumn 45, Issue 4, 2007, Pages 415-419

Deracemization of (RS)-1-[(4-methylselanyl)phenyl]ethanol and (RS)-1-[(4-ethylselanyl)phenyl]ethanol by strains of Aspergillus terreus

Author keywords

Aspergillus terreus; Biotransformation; Chiral organoseleno alcohols; Deracemization; Fungal cells

Indexed keywords

ASPERGILLUS TERREUS; BIOTRANSFORMATION; DE-RACEMIZATION; DIFFERENT MASS; ENANTIOMERIC EXCESS; FUNGAL CELLS; FUNGAL STRAINS; PRODUCT YIELDS;

EID: 40749096469     PISSN: 13309862     EISSN: 13342606     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (14)

References (11)
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  • 3
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    • M. Tiecco: Organoselenium Chemistry: Modern Developments in Organic Synthesis (Topics in Current Chemistry). In: Electrophilic Selenium, Selenocyclizations, T. Wirth (Ed.), Springer-Verlag, Heidelberg, Germany (2000).
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  • 5
    • 2442450566 scopus 로고    scopus 로고
    • Asymmetric synthesis of arylseleno alcohols by means of the reduction of organoseleno acetophenones by whole fungal cells
    • L.H. Andrade, A.T. Omori, A.L.M. Porto, J.V. Comasseto, Asymmetric synthesis of arylseleno alcohols by means of the reduction of organoseleno acetophenones by whole fungal cells, J. Mol. Catal. B-Enzym. 29 (2004) 47-54.
    • (2004) J. Mol. Catal. B-Enzym , vol.29 , pp. 47-54
    • Andrade, L.H.1    Omori, A.T.2    Porto, A.L.M.3    Comasseto, J.V.4
  • 6
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    • Preparation of chiral organochalcogeno-α-methylbenzyl alcohols via biocatalysis. The role of Daucus carota root
    • J.V. Comasseto, A.T. Omori, A.L.M. Porto, L.H. Andrade, Preparation of chiral organochalcogeno-α-methylbenzyl alcohols via biocatalysis. The role of Daucus carota root, Tetrahedron Lett. 45 (2004) 473-476.
    • (2004) Tetrahedron Lett , vol.45 , pp. 473-476
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  • 8
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    • Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase - Novozyme 435
    • A.T. Omori, L.F. Assis, L.H. Andrade, J.V. Comasseto, A.L.M. Porto, Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase - Novozyme 435, Tetrahedron: Asymmetry, 18 (2007) 1048-1053.
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  • 9
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    • Deracemization of aryl ethanols and reduction of acetophenones by whole fungal cells of Aspergillus terreus CCT 4083, A. terreus CCT 3320 and Rhizopus oryzae CCT 4964
    • J.V. Comasseto, L.H. Andrade, A.T. Omori, L.F. Assis, A.L.M. Porto, Deracemization of aryl ethanols and reduction of acetophenones by whole fungal cells of Aspergillus terreus CCT 4083, A. terreus CCT 3320 and Rhizopus oryzae CCT 4964, J. Mol. Catal. B-Enzym. 29 (2004) 55-61.
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  • 10
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    • J.V. Comasseto, L.F. Assis, L.H. Andrade, I.H. Schoenlein-Crusius, A.L.M. Porto, Biotransformations of ortho-, meta-and para-aromatic nitrocompounds by strains of Aspergillus terreus: Reduction of ketones and deracemization of alcohols, J. Mol. Catal. B-Enzym. 39 (2006) 24-30.
    • J.V. Comasseto, L.F. Assis, L.H. Andrade, I.H. Schoenlein-Crusius, A.L.M. Porto, Biotransformations of ortho-, meta-and para-aromatic nitrocompounds by strains of Aspergillus terreus: Reduction of ketones and deracemization of alcohols, J. Mol. Catal. B-Enzym. 39 (2006) 24-30.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.