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

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F11%3A10113695" target="_blank" >RIV/00216208:11310/11:10113695 - isvavai.cz</a>
Alternative codes found
RIV/61989592:15310/11:33118288 RIV/61388963:_____/11:00361378 RIV/68407700:21340/11:00183634
Result on the web
<a href="http://dx.doi.org/10.1016/j.tetasy.2011.05.017" target="_blank" >http://dx.doi.org/10.1016/j.tetasy.2011.05.017</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.tetasy.2011.05.017" target="_blank" >10.1016/j.tetasy.2011.05.017</a>

Result language
angličtina
Original language name
Study of stereoselectivity of reduction of 18-oxo des-E triterpenoids by sodium borohydride in the presence of cerium chloride
Original language description
Stereoselectivity of the reduction of the 18-oxo group in cytotoxically active des-E lupane derivatives was described. It was found that the stereoselectivity of the reduction of the 18-keto group both depended on the type and length of the substituent chain at the position 17.
Czech name
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Czech description
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Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
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Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2011
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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