The Reactivity Study on N3,N3-(3-Oxapentan-1,5-diyl)-N1-(2-phenyl-3,4-dihydroquinazolin-4-yliden)thiourea

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F01%3A00005300" target="_blank" >RIV/00216224:14310/01:00005300 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Result language
angličtina
Original language name
The Reactivity Study on N3,N3-(3-Oxapentan-1,5-diyl)-N1-(2-phenyl-3,4-dihydroquinazolin-4-yliden)thiourea
Original language description
The thioamide represented by the model compound N3,N3-(3-oxapentan-1,5-diyl)-N1-(2-phenyl-3,4-dihydro-quinazolin-4-ylidene)thiourea contain both multi-functional nucleophilic and electrophilic characters. It reacts regioselectivity with amines, amines inthe presence of H2O2 and alkyl halides to give the transamination reaction products, the oxidative desulfurization products and the S-alkyl product, respectively. FTIR, 1H NMR, 13C NMR, mass spectroscopy and X-ray identified compounds.
Czech name
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Czech description
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Project
<a href="/en/project/GA203%2F01%2F1333" target="_blank" >GA203/01/1333: Chalcogen organic compounds - synthesis, transformation and structure elucidation</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year
2001
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Article name in the collection
Proceedings of ECSOC-5, The Fifth International Electronic Conference on Synthetic Organic Chemistry, http://www.mdpi.org/ecsoc-5.htm
ISBN
3-906980-06-5
ISSN
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e-ISSN
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Number of pages
1
Pages from-to
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Publisher name
MDPI, Basel, Switzerland
Place of publication
Basel
Event location
Basel
Event date
Jan 1, 2001
Type of event by nationality
WRD - Celosvětová akce
UT code for WoS article
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