Reduction of some cyclic derivatives of diphenic acid with sodium borane in alcohols; Bulletin of the Tomsk Polytechnic University; Vol. 311, № 3

Reduction of some cyclic derivatives of diphenic acid with sodium borane in alcohols; Bulletin of the Tomsk Polytechnic University; Vol. 311, № 3

Xehetasun bibliografikoak
Parent link:	Bulletin of the Tomsk Polytechnic University/ Tomsk Polytechnic University (TPU).— , 2006-2007 Vol. 311, № 3.— 2007.— [P. 93-97]
Beste egile batzuk:	Yanovskiy V. A., Baturin D. M., Yagovkin A. Yu., Bakibaev A. A. Abdigali Abdimanapovich
Gaia:	Заглавие с титульного листа Электронная версия печатной публикации Reduction of heptamerous cyclic imides with sodium borane has been carried out for the first time by the example of some imides of diphenic acid. In this case for the first time amides of 2'-hydroxymethylxenyl-2-carboxylic acid which are potentially valued bioactive compounds were obtained. It was shown that the nature of substituent at nitrogen atom influences the reaction products yields and composition. The reduction of diphenic acid anhydride with sodium borane in simple alcohols occurs with the formation of reduction products - 7H-dibenzyl[c,e] oxepin-5-on (36...46 %) as well as products of diphenic acid alcoholysis-monoester (29...36 %). In this case the nature of alcohol influences weakly reaction products ratio
Hizkuntza:	ingelesa
Argitaratua:	2007
Saila:	Chemistry
Gaiak:	reduction diphenic acid sodium borane alcohols heptamerous cyclic amides bioactive compounds nitrogen atoms substituent products compositions formation труды учёных ТПУ электронный ресурс
Sarrera elektronikoa:	http://www.lib.tpu.ru/fulltext/v/Bulletin_TPU/2007/v311eng/i3/25.pdf
Formatua:	Baliabide elektronikoa Liburu kapitulua
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=183008

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