Tritylamine as an ammonia synthetic equivalent: preparation of primary amides

Theodorou, V.; Karkatsoulis, A.; Kinigopoulou, M.; Ragoussis, V.; Skobridis, K.

Tritylamine as an ammonia synthetic equivalent: preparation of primary amides

dc.contributor.author	Theodorou, V.	en
dc.contributor.author	Karkatsoulis, A.	en
dc.contributor.author	Kinigopoulou, M.	en
dc.contributor.author	Ragoussis, V.	en
dc.contributor.author	Skobridis, K.	en
dc.date.accessioned	2015-11-24T16:51:51Z
dc.date.available	2015-11-24T16:51:51Z
dc.identifier.issn	1424-6376	-
dc.identifier.uri	https://olympias.lib.uoi.gr/jspui/handle/123456789/9794
dc.rights	Default Licence	-
dc.subject	tritylamine	en
dc.subject	tritylamides	en
dc.subject	ammonia synthetic equivalent	en
dc.subject	synthesis of primary amides	en
dc.subject	detritylation	en
dc.subject	palladium-catalyzed carbonylation	en
dc.subject	base-induced rearrangement	en
dc.subject	protected amino-acids	en
dc.subject	peptide-synthesis	en
dc.subject	organic-synthesis	en
dc.subject	carboxylic-acids	en
dc.subject	facile synthesis	en
dc.subject	aqueous-media	en
dc.subject	esters	en
dc.subject	triphenylmethylamine	en
dc.title	Tritylamine as an ammonia synthetic equivalent: preparation of primary amides	en
heal.abstract	A new synthetic route to primary amides via N-tritylamides was developed. The initially formed N-tritylamides, derived from acylation of tritylamine by activated carboxylic acid derivatives, were deprotected with trifluoroacetic acid at room temperature to the desired primary amides in good yields.	en
heal.access	campus	-
heal.fullTextAvailability	TRUE	-
heal.identifier.secondary	<Go to ISI>://000271148800025	-
heal.journalName	Arkivoc	en
heal.journalType	peer reviewed	-
heal.language	en	-
heal.publicationDate	2009	-
heal.recordProvider	Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας	el
heal.type	journalArticle	-
heal.type.el	Άρθρο Περιοδικού	el
heal.type.en	Journal article	en

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