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Volumn , Issue 31, 2007, Pages 5175-5179

Enantioselective one-pot two-step synthesis of hydrophobic allylic alcohols in aqueous medium through the combination of a Wittig reaction and an enzymatic ketone reduction

Author keywords

Alcohols; Chemoenzymatic synthesis; Enzyme catalysis; Reduction; Wittig reactions

Indexed keywords


EID: 35948960796     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200700647     Document Type: Article
Times cited : (31)

References (49)
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    • The (S)-alcohol dehydrogenase from Rhodococcus sp., recombinant in E. coli, was developed in the research group of Prof. Dr. Werner Hummel and is available as a commercial enzyme formulation from EVOcatal GmbH, Merowinger Platz la, 40225 Düsseldorf, Germany; internet: http://www.evocatal.com
    • The (S)-alcohol dehydrogenase from Rhodococcus sp., recombinant in E. coli, was developed in the research group of Prof. Dr. Werner Hummel and is available as a commercial enzyme formulation from EVOcatal GmbH, Merowinger Platz la, 40225 Düsseldorf, Germany; internet: http://www.evocatal.com
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    • For other alcohol dehydrogenases suitable as a catalyst for the reduction of α,β-unsaturated ketones, see, for example, ref.[1b
    • [1b]


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.