Hydantoins as Anticonvulsants. III. 5-Alkoxy- and Aryloxymethyl-5-(2-Thienyl) Hydantoins

It has been shown in the case of a compound synthesized in this laboratory that substitution of the thienyl group for one of the phenyl groups in diphenyl hydantoin produces a compound with less toxicity and somewhat greater activity. It was considered of interest to carry out an analogous substitut...

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Main Author: Sadler, Jack W.
Other Authors: Spurlock, J. J.
Format: Others
Language:English
Published: North Texas State College 1950
Subjects:
Online Access:https://digital.library.unt.edu/ark:/67531/metadc83665/
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spelling ndltd-unt.edu-info-ark-67531-metadc836652017-03-17T08:39:37Z Hydantoins as Anticonvulsants. III. 5-Alkoxy- and Aryloxymethyl-5-(2-Thienyl) Hydantoins Sadler, Jack W. hydantoins 5-alkoxy- and aryloxymethyl-5-(2-thienyl) hydantoins Hydantoin. Anticonvulsants. It has been shown in the case of a compound synthesized in this laboratory that substitution of the thienyl group for one of the phenyl groups in diphenyl hydantoin produces a compound with less toxicity and somewhat greater activity. It was considered of interest to carry out an analogous substitution in the series of 5-phenyl-5-alkoxymethylhydantions. North Texas State College Spurlock, J. J. Carrico, James L. 1950 Thesis or Dissertation iv, 22 leaves : ill. Text call-no: 379 N81 no.1588 local-cont-no: n_01588 untcat: b2477094 https://digital.library.unt.edu/ark:/67531/metadc83665/ ark: ark:/67531/metadc83665 English Public Copyright Copyright is held by the author, unless otherwise noted. All rights reserved. Sadler, Jack W.
collection NDLTD
language English
format Others
sources NDLTD
topic hydantoins
5-alkoxy- and aryloxymethyl-5-(2-thienyl) hydantoins
Hydantoin.
Anticonvulsants.
spellingShingle hydantoins
5-alkoxy- and aryloxymethyl-5-(2-thienyl) hydantoins
Hydantoin.
Anticonvulsants.
Sadler, Jack W.
Hydantoins as Anticonvulsants. III. 5-Alkoxy- and Aryloxymethyl-5-(2-Thienyl) Hydantoins
description It has been shown in the case of a compound synthesized in this laboratory that substitution of the thienyl group for one of the phenyl groups in diphenyl hydantoin produces a compound with less toxicity and somewhat greater activity. It was considered of interest to carry out an analogous substitution in the series of 5-phenyl-5-alkoxymethylhydantions.
author2 Spurlock, J. J.
author_facet Spurlock, J. J.
Sadler, Jack W.
author Sadler, Jack W.
author_sort Sadler, Jack W.
title Hydantoins as Anticonvulsants. III. 5-Alkoxy- and Aryloxymethyl-5-(2-Thienyl) Hydantoins
title_short Hydantoins as Anticonvulsants. III. 5-Alkoxy- and Aryloxymethyl-5-(2-Thienyl) Hydantoins
title_full Hydantoins as Anticonvulsants. III. 5-Alkoxy- and Aryloxymethyl-5-(2-Thienyl) Hydantoins
title_fullStr Hydantoins as Anticonvulsants. III. 5-Alkoxy- and Aryloxymethyl-5-(2-Thienyl) Hydantoins
title_full_unstemmed Hydantoins as Anticonvulsants. III. 5-Alkoxy- and Aryloxymethyl-5-(2-Thienyl) Hydantoins
title_sort hydantoins as anticonvulsants. iii. 5-alkoxy- and aryloxymethyl-5-(2-thienyl) hydantoins
publisher North Texas State College
publishDate 1950
url https://digital.library.unt.edu/ark:/67531/metadc83665/
work_keys_str_mv AT sadlerjackw hydantoinsasanticonvulsantsiii5alkoxyandaryloxymethyl52thienylhydantoins
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