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Tritylamine as an ammonia synthetic equivalent: Preparation of primary amides

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Tritylamine as an ammonia synthetic equivalent: Preparation of primary amides
Theodorou, V. Karkatsoulis, A. Kinigopoulou, M. Ragoussis, V. Skobridisa, K.
scientific_publication_article
Επιστημονική δημοσίευση - Άρθρο Περιοδικού (EL)
Scientific publication - Journal Article (EN)
2009
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. © ARKAT USA, Inc. (EN)
English
Ερευνητικό υλικό ΕΚΠΑ
https://creativecommons.org/licenses/by-nc/4.0/
University of Athens
Pergamos Digital Library
Journal Article



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