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Volumn 44, Issue 4, 2003, Pages 801-804

Process for preparing Ezetimibe intermediate by an acid enhanced chemo- and enantioselective CBS catalyzed ketone reduction

Author keywords

Asymmetric ketone reduction; Ezetimibe; R MeCBS

Indexed keywords

ACID; ALCOHOL; ANTILIPEMIC AGENT; BORANE DERIVATIVE; CARBONYL DERIVATIVE; CHEMICAL COMPOUND; EZETIMIBE; KETONE DERIVATIVE; REDUCING AGENT; SCAVENGER; SODIUM BOROHYDRIDE; TETRAHYDROFURAN DERIVATIVE; WATER;

EID: 0037454990     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)02700-4     Document Type: Article
Times cited : (43)

References (21)
  • 21
    • 0037012945 scopus 로고    scopus 로고
    • 4 stabilizer in BTHF on CBS catalyzed reduction was simultaneously studied in Callery Chemical Company. Lewis acids were also demonstrated enhancing the selectivity significantly
    • 4 stabilizer in BTHF on CBS catalyzed reduction was simultaneously studied in Callery Chemical Company. Lewis acids were also demonstrated enhancing the selectivity significantly. Nettles S.M., Matos K., Burkhardt E.R., Rouda D.R., Corella J.A. J. Org. Chem. 67:2002;2970.
    • (2002) J. Org. Chem. , vol.67 , pp. 2970
    • Nettles, S.M.1    Matos, K.2    Burkhardt, E.R.3    Rouda, D.R.4    Corella, J.A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.