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Volumn 65, Issue 3, 2010, Pages 337-340

Enantioselective biocatalytic reduction of non-protected hydroxyacetophenones

Author keywords

Alcohols; Asymmetric synthesis; Biocatalysis; Enzymes; Reduction

Indexed keywords

ALCOHOLS; ENZYMES; KETONES; REDUCTION;

EID: 77953813181     PISSN: 09320776     EISSN: None     Source Type: Journal    
DOI: 10.1515/znb-2010-0317     Document Type: Article
Times cited : (8)

References (26)
  • 8
    • 33748530708 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 5677-5681
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 5677-5681
  • 13
    • 56749093129 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 9551-9554
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 9551-9554
  • 15
    • 72949100542 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 9355-9358
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9355-9358
  • 16
    • 37049079343 scopus 로고
    • Such a strategy based on protection of the hydroxy group in ́-hydroxyacetophenone, asymmetric reduction with a chiral chlorodialkylborane and in situ-deprotection has been applied for the synthesis of (S)-l-(4-hydroxyphenyl)ethan-l-ol: E.T. Everhart, J.C. Craig, J. Chem. Soc, Perkin Trans. 1991, 1, 1701-1707.
    • (1991) J. Chem. Soc, Perkin Trans. , vol.1 , pp. 1701-1707
    • Everhart, E.T.1    Craig, J.C.2
  • 26
    • 77953828768 scopus 로고    scopus 로고
    • Available as commercial product (product number 1.1.030) from evocatal GmbH, Merowinger Platz la, 40225 D̈sseldorf, Germany. See also
    • Available as commercial product (product number 1.1.030) from evocatal GmbH, Merowinger Platz la, 40225 D̈sseldorf, Germany. See also: http://www.evocatal.com.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.