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Synthesis and characterization of new dialkylacylphosphonylhydrazones

The present work refers to the synthesis of novel dialkylacylphosphonylhydrazones that occurs in three reaction steps: the first one is the synthesis of different dialkyl acetate phosphonoacetates obtained by the reaction of ethyl bromoacetate with the trialkyl phosphite of interest. The second one...

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Detalles Bibliográficos
Autores principales: Barboza, Henriqueta Talita Guimarães, Soares, Antonio Gomes, Freitas-Silva, Otniel, DaCosta, João Batista Neves
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6146382/
https://www.ncbi.nlm.nih.gov/pubmed/30246110
http://dx.doi.org/10.1016/j.dib.2018.08.073
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author Barboza, Henriqueta Talita Guimarães
Soares, Antonio Gomes
Freitas-Silva, Otniel
DaCosta, João Batista Neves
author_facet Barboza, Henriqueta Talita Guimarães
Soares, Antonio Gomes
Freitas-Silva, Otniel
DaCosta, João Batista Neves
author_sort Barboza, Henriqueta Talita Guimarães
collection PubMed
description The present work refers to the synthesis of novel dialkylacylphosphonylhydrazones that occurs in three reaction steps: the first one is the synthesis of different dialkyl acetate phosphonoacetates obtained by the reaction of ethyl bromoacetate with the trialkyl phosphite of interest. The second one is the synthesis of acetic diethoxyphosphonylhydrazines which is from the reaction between the synthesized dialkyl phosphonoacetates and hydrazine. The third and final steps is the condensation of acetic diethoxyphosphonylhydrazides with different heterocyclic aldehydes. In total, 17 unpublished compounds, namely 1 to 17 (Table 1) were obtained with a diastereoisomeric mixture of the preferential conformation E and all the compounds were characterized by 1-H and 13-C and 31-P NMR, infrared (IR) and mass spectroscopy (MS). This work presents the characterization data of these compounds.
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spelling pubmed-61463822018-09-21 Synthesis and characterization of new dialkylacylphosphonylhydrazones Barboza, Henriqueta Talita Guimarães Soares, Antonio Gomes Freitas-Silva, Otniel DaCosta, João Batista Neves Data Brief Data Article The present work refers to the synthesis of novel dialkylacylphosphonylhydrazones that occurs in three reaction steps: the first one is the synthesis of different dialkyl acetate phosphonoacetates obtained by the reaction of ethyl bromoacetate with the trialkyl phosphite of interest. The second one is the synthesis of acetic diethoxyphosphonylhydrazines which is from the reaction between the synthesized dialkyl phosphonoacetates and hydrazine. The third and final steps is the condensation of acetic diethoxyphosphonylhydrazides with different heterocyclic aldehydes. In total, 17 unpublished compounds, namely 1 to 17 (Table 1) were obtained with a diastereoisomeric mixture of the preferential conformation E and all the compounds were characterized by 1-H and 13-C and 31-P NMR, infrared (IR) and mass spectroscopy (MS). This work presents the characterization data of these compounds. Elsevier 2018-08-30 /pmc/articles/PMC6146382/ /pubmed/30246110 http://dx.doi.org/10.1016/j.dib.2018.08.073 Text en © 2018 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Data Article
Barboza, Henriqueta Talita Guimarães
Soares, Antonio Gomes
Freitas-Silva, Otniel
DaCosta, João Batista Neves
Synthesis and characterization of new dialkylacylphosphonylhydrazones
title Synthesis and characterization of new dialkylacylphosphonylhydrazones
title_full Synthesis and characterization of new dialkylacylphosphonylhydrazones
title_fullStr Synthesis and characterization of new dialkylacylphosphonylhydrazones
title_full_unstemmed Synthesis and characterization of new dialkylacylphosphonylhydrazones
title_short Synthesis and characterization of new dialkylacylphosphonylhydrazones
title_sort synthesis and characterization of new dialkylacylphosphonylhydrazones
topic Data Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6146382/
https://www.ncbi.nlm.nih.gov/pubmed/30246110
http://dx.doi.org/10.1016/j.dib.2018.08.073
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