The Wohl Reaction Applied to Some Benzoylated Aldononitriles

Hexa-O-benozyl-D-glycerogulo-heptonomtrile (III), hexa-O-benzoyl-D-glycero-L-mareno-heptononitrile (IV), D-glycero-D-galacto-heptose oxime (V), and, from this last compound, hexa,-O-benzoyl-D-glycero-D-galacto-heptononitrile (VI) were prepared; these nitriles were treated with methanolic ammonia. Fr...

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Autores principales: Deferrari, J.O., Matsuhiro, B.
Formato: JOUR
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00223263_v31_n3_p905_Deferrari
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Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires
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spelling todo:paper_00223263_v31_n3_p905_Deferrari2023-10-03T14:31:14Z The Wohl Reaction Applied to Some Benzoylated Aldononitriles Deferrari, J.O. Matsuhiro, B. Hexa-O-benozyl-D-glycerogulo-heptonomtrile (III), hexa-O-benzoyl-D-glycero-L-mareno-heptononitrile (IV), D-glycero-D-galacto-heptose oxime (V), and, from this last compound, hexa,-O-benzoyl-D-glycero-D-galacto-heptononitrile (VI) were prepared; these nitriles were treated with methanolic ammonia. From III, l,l-bis(ben-zamido)-l-deoxy-D-glucitol,. N-benzoyl-β-D-glucopyranosylamine, and D-glucose were obtained. From IV, 1,1-bis(benzamido)-l-deoxy-D-galactitol, N-benzoyl-β-D-galactopyranosylamine, and D-galactose were obtained. From VI, l,l-bis(benzamido)-l-deoxy-D-mannitol, Arbenzoyl-β-D-mannopyranosylamine, and D-mannose were obtained. © 1966, American Chemical Society. All rights reserved. Fil:Deferrari, J.O. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Matsuhiro, B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00223263_v31_n3_p905_Deferrari
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description Hexa-O-benozyl-D-glycerogulo-heptonomtrile (III), hexa-O-benzoyl-D-glycero-L-mareno-heptononitrile (IV), D-glycero-D-galacto-heptose oxime (V), and, from this last compound, hexa,-O-benzoyl-D-glycero-D-galacto-heptononitrile (VI) were prepared; these nitriles were treated with methanolic ammonia. From III, l,l-bis(ben-zamido)-l-deoxy-D-glucitol,. N-benzoyl-β-D-glucopyranosylamine, and D-glucose were obtained. From IV, 1,1-bis(benzamido)-l-deoxy-D-galactitol, N-benzoyl-β-D-galactopyranosylamine, and D-galactose were obtained. From VI, l,l-bis(benzamido)-l-deoxy-D-mannitol, Arbenzoyl-β-D-mannopyranosylamine, and D-mannose were obtained. © 1966, American Chemical Society. All rights reserved.
format JOUR
author Deferrari, J.O.
Matsuhiro, B.
spellingShingle Deferrari, J.O.
Matsuhiro, B.
The Wohl Reaction Applied to Some Benzoylated Aldononitriles
author_facet Deferrari, J.O.
Matsuhiro, B.
author_sort Deferrari, J.O.
title The Wohl Reaction Applied to Some Benzoylated Aldononitriles
title_short The Wohl Reaction Applied to Some Benzoylated Aldononitriles
title_full The Wohl Reaction Applied to Some Benzoylated Aldononitriles
title_fullStr The Wohl Reaction Applied to Some Benzoylated Aldononitriles
title_full_unstemmed The Wohl Reaction Applied to Some Benzoylated Aldononitriles
title_sort wohl reaction applied to some benzoylated aldononitriles
url http://hdl.handle.net/20.500.12110/paper_00223263_v31_n3_p905_Deferrari
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AT matsuhirob thewohlreactionappliedtosomebenzoylatedaldononitriles
AT deferrarijo wohlreactionappliedtosomebenzoylatedaldononitriles
AT matsuhirob wohlreactionappliedtosomebenzoylatedaldononitriles
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