POTÁČEK, Milan, Lukáš RÝČEK, Romano ORRU and Stanislav MAN. Microwave initiated in situ formed azomethine ylides from variously substituted allyloxy naphtahalene carbaldehydes and secondary amines in intramolecular 1,3-dipolar cycloadditions. In Book of Abstracts COST Action D32 Final Meeting. Krakow: Department of Chemistry and Technology of Polymers, Krakow University of Technology, 2009, p. 106-108, 2 pp. ISBN 978-83-928784-0-7.
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Basic information
Original name Microwave initiated in situ formed azomethine ylides from variously substituted allyloxy naphtahalene carbaldehydes and secondary amines in intramolecular 1,3-dipolar cycloadditions
Name in Czech Mikrovlnami iniciované in situ vytvořené azomethinylidy vznikající z různě substituovaných allyloxy naftalenaldehydů a sekundárních aminů při intramolekulární 1,3-dipolární cykloadici
Authors POTÁČEK, Milan (203 Czech Republic, guarantor), Lukáš RÝČEK (203 Czech Republic), Romano ORRU (528 Netherlands) and Stanislav MAN (203 Czech Republic).
Edition Krakow, Book of Abstracts COST Action D32 Final Meeting, p. 106-108, 2 pp. 2009.
Publisher Department of Chemistry and Technology of Polymers, Krakow University of Technology
Other information
Original language English
Type of outcome Proceedings paper
Field of Study 10401 Organic chemistry
Country of publisher Poland
Confidentiality degree is not subject to a state or trade secret
RIV identification code RIV/00216224:14310/09:00035312
Organization unit Faculty of Science
ISBN 978-83-928784-0-7
Keywords in English microwave; cycloaddition; stereochemistry
Tags cycloaddition, microwave, stereochemistry
Tags International impact, Reviewed
Changed by Changed by: prof. RNDr. Milan Potáček, CSc., učo 638. Changed: 8/4/2010 09:04.
Abstract
Application of microwave in intramolecular 1,3-dipolar cycloaddition and stereospecifity of the reactions. Reactions were ivestigated at variously substituted naphtalene skeletons bearing in alfa, beta positions aldehyde and allyloxy groups with secondary amines.
Abstract (in Czech)
Intramolekulární 1,3- dipolární cykloadice iniciovaná mikrovlnami a sledování stereospecifity reakcí.Reakce byly prováděny na různě alfa, beta substituovaných systémech nesoucích aldehydickou a allyloxy skupinu se sekundárními aminy.
Links
OC08052, research and development projectName: Mikrovlnami iniciované syntézy (Acronym: MICROSYNT)
Investor: Ministry of Education, Youth and Sports of the CR, Microwave initiated syntheses
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