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Volumn 2016, Issue 19, 2016, Pages 3162-3165

Chemoenzymatic Synthesis of δ-Keto β-Hydroxy Esters as Useful Intermediates for Preparing Statins

Author keywords

Asymmetric synthesis; Enzymes; Inhibitors; Ketones; Reduction; Statins

Indexed keywords


EID: 84970965892     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201600268     Document Type: Article
Times cited : (13)

References (44)
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    • Acetalization experiments were performed by using ethylene glycol or 1,2-bis(trimethylsiloxy)ethane in toluene or cyclohexane in the presence of several Brønsted and Lewis acid catalysts. However, transesterification of the methyl ester group was the most favored process under the acetalization conditions, However, transesterification of the methyl ester group was the most favored process under the acetalization conditions
    • Acetalization experiments were performed by using ethylene glycol or 1,2-bis(trimethylsiloxy)ethane in toluene or cyclohexane in the presence of several Brønsted and Lewis acid catalysts. However, transesterification of the methyl ester group was the most favored process under the acetalization conditions
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    • (2002) Angew. Chem. , vol.114 , pp. 1246-1250
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.