A New Allenyloxime Synthon in Heterocyclizations Leading to Stable Cyclic Nitrones
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F08%3A00051051" target="_blank" >RIV/00216224:14310/08:00051051 - isvavai.cz</a>
Result on the web
<a href="http://www.chemicke-listy.cz/docs/full/2008_11_1021-1083.pdf" target="_blank" >http://www.chemicke-listy.cz/docs/full/2008_11_1021-1083.pdf</a>
DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
A New Allenyloxime Synthon in Heterocyclizations Leading to Stable Cyclic Nitrones
Original language description
A variety of conditions including reductive and/or basic reagents in aqueous or alcoholic solution was applied to 2,2-dimethylpenta-3,4-dienal oxime. Formation of various five-membered heterocycles with excellent chemical selectivity was observed. Most of the reactions yielded cyclic nitrones with stable dipolar structure and unique functionalities present. All products of cyclization were isolated and fully characterized.
Czech name
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Czech description
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Classification
Type
O - Miscellaneous
CEP classification
CC - Organic chemistry
OECD FORD branch
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Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2008
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů