Conformation study of a-ring in 19β,28-epoxy-2-fluoro-18α-oleananes
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F49777513%3A23420%2F06%3A00000003" target="_blank" >RIV/49777513:23420/06:00000003 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Conformation study of a-ring in 19β,28-epoxy-2-fluoro-18α-oleananes
Original language description
A series of 2-fluoro-substituted 19ß,28-epoxy-18α-oleanane triterpenoids was prepared. Detailed NMR analysis (1H, 13C, 19F) was used for independent determination of the configuration of substituents. Conformation of the A-ring was derived from coupling constants J(H,H), J(F,H), J(F,C) and NOE-contacts observed in 2D-H,H-NOESY spectra. It was found that A-ring in all 2α-fluoro derivatives and 2ß-fluoro-3ß-OR derivatives and adopts chair-form, while in 2ß-fluoro ketone a boat-form is preferred.The chair–boat equilibrium of A-ring was found in 2ß-fluoro-3.-OR derivatives.
Czech name
Konformační studie a-kruhu 19β,28-epoxy-2-fluoro-18α-oleananů.
Czech description
Byla připravena řada triterpenoidních 2-flouro substituentů 19ß,28-epoxy-18beta-oleananu. Podrobnou NMR analýzou byla určena konfigurace substituentů.
Classification
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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Result continuities
Project
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Continuities
S - Specificky vyzkum na vysokych skolach
Others
Publication year
2006
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Collection of Czechoslovak Chemical Communications
ISSN
0010-0765
e-ISSN
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Volume of the periodical
71
Issue of the periodical within the volume
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Country of publishing house
CZ - CZECH REPUBLIC
Number of pages
19
Pages from-to
368
UT code for WoS article
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EID of the result in the Scopus database
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