Cyclization of Hydrazones of 2-Acetyl-1-naphthol and 1-Acetyl-2-naphthol with Triphosgene. Synthesis of Spiro Naphthoxazine Dimers

Cyclization of hydrazones derived from 2-acetyl-1-naphthol and 1-acetyl-2-naphthol with triphosgene gave naphtho[1,2-e]-1,3-oxazines, naphtho[2,1-e]-1,3-oxazines or their spiro dimers depending on the molar ratio of triphosgene used for the cyclization.

Detalles Bibliográficos
Autores principales: Al-Bogami, Abdullah Saad, Al-Majid, Abdullah Mohammed, Al-Saad, Mohammed Ali, Mousa, Ahmed Amine, Al-Mazroa, Sara Abdullah, Alkhathlan, Hamad Zaid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2009
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254203/
https://www.ncbi.nlm.nih.gov/pubmed/19553888
http://dx.doi.org/10.3390/molecules14062147
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author Al-Bogami, Abdullah Saad
Al-Majid, Abdullah Mohammed
Al-Saad, Mohammed Ali
Mousa, Ahmed Amine
Al-Mazroa, Sara Abdullah
Alkhathlan, Hamad Zaid
author_facet Al-Bogami, Abdullah Saad
Al-Majid, Abdullah Mohammed
Al-Saad, Mohammed Ali
Mousa, Ahmed Amine
Al-Mazroa, Sara Abdullah
Alkhathlan, Hamad Zaid
author_sort Al-Bogami, Abdullah Saad
collection PubMed
description Cyclization of hydrazones derived from 2-acetyl-1-naphthol and 1-acetyl-2-naphthol with triphosgene gave naphtho[1,2-e]-1,3-oxazines, naphtho[2,1-e]-1,3-oxazines or their spiro dimers depending on the molar ratio of triphosgene used for the cyclization.
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spelling pubmed-62542032018-11-30 Cyclization of Hydrazones of 2-Acetyl-1-naphthol and 1-Acetyl-2-naphthol with Triphosgene. Synthesis of Spiro Naphthoxazine Dimers Al-Bogami, Abdullah Saad Al-Majid, Abdullah Mohammed Al-Saad, Mohammed Ali Mousa, Ahmed Amine Al-Mazroa, Sara Abdullah Alkhathlan, Hamad Zaid Molecules Article Cyclization of hydrazones derived from 2-acetyl-1-naphthol and 1-acetyl-2-naphthol with triphosgene gave naphtho[1,2-e]-1,3-oxazines, naphtho[2,1-e]-1,3-oxazines or their spiro dimers depending on the molar ratio of triphosgene used for the cyclization. Molecular Diversity Preservation International 2009-06-12 /pmc/articles/PMC6254203/ /pubmed/19553888 http://dx.doi.org/10.3390/molecules14062147 Text en © 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Al-Bogami, Abdullah Saad
Al-Majid, Abdullah Mohammed
Al-Saad, Mohammed Ali
Mousa, Ahmed Amine
Al-Mazroa, Sara Abdullah
Alkhathlan, Hamad Zaid
Cyclization of Hydrazones of 2-Acetyl-1-naphthol and 1-Acetyl-2-naphthol with Triphosgene. Synthesis of Spiro Naphthoxazine Dimers
title Cyclization of Hydrazones of 2-Acetyl-1-naphthol and 1-Acetyl-2-naphthol with Triphosgene. Synthesis of Spiro Naphthoxazine Dimers
title_full Cyclization of Hydrazones of 2-Acetyl-1-naphthol and 1-Acetyl-2-naphthol with Triphosgene. Synthesis of Spiro Naphthoxazine Dimers
title_fullStr Cyclization of Hydrazones of 2-Acetyl-1-naphthol and 1-Acetyl-2-naphthol with Triphosgene. Synthesis of Spiro Naphthoxazine Dimers
title_full_unstemmed Cyclization of Hydrazones of 2-Acetyl-1-naphthol and 1-Acetyl-2-naphthol with Triphosgene. Synthesis of Spiro Naphthoxazine Dimers
title_short Cyclization of Hydrazones of 2-Acetyl-1-naphthol and 1-Acetyl-2-naphthol with Triphosgene. Synthesis of Spiro Naphthoxazine Dimers
title_sort cyclization of hydrazones of 2-acetyl-1-naphthol and 1-acetyl-2-naphthol with triphosgene. synthesis of spiro naphthoxazine dimers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254203/
https://www.ncbi.nlm.nih.gov/pubmed/19553888
http://dx.doi.org/10.3390/molecules14062147
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