Study of stereoselectivity of reduction of 18-oxo des-E triterpenoids by sodium borohydride in the presence of cerium chloride

Tetrahedron Asymmetry

Volumn 22, Issue 9, 2011, Pages 1011-1020

  Kvasnica, Miroslav ^a   Sarek, Jan ^b   Vlk, Martin ^b,c   Budesinsky, Milos ^a   Stepanek, Ondrej ^a   Kubelka, Tomas ^a   Plutnarova, Iva ^d  

^a INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY   (Czech Republic)

^b PALACKÝ UNIVERSITY   (Czech Republic)

^c CZECH TECHNICAL UNIVERSITY IN PRAGUE   (Czech Republic)

^d CHARLES UNIVERSITY   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

3 BETA HYDROXY 18 OXO 19,20,28,29,30 PENTANOR 17 ALPHA H LUPAN 21 OIC ACID; ALCOHOL DERIVATIVE; BETA KETOACID; CARBOXYL GROUP; CERIUM; CERIUM CHLORIDE; HEPTANORKETONE; METHYLENE KETONE; SODIUM BOROHYDRIDE; TRITERPENOID; UNCLASSIFIED DRUG;

ARTICLE; CYTOTOXICITY; DERIVATIZATION; DRUG ACETYLATION; DRUG STRUCTURE; DRUG TRANSFORMATION; PRIORITY JOURNAL; REDUCTION; STEREOCHEMISTRY;

EID: 79960938713     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2011.05.017     Document Type: Article

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