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Merging catalyst-free synthesis and iodine catalysis: one-pot synthesis of dihydrofuropyrimidines and spirodihydrofuropyrimidine pyrazolones

A new and efficient one-pot strategy combining catalyst-free synthesis and iodine catalysis has been developed for the synthesis of dihydrofuropyrimidines and spirodihydrofuropyrimidine pyrazolones. This approach affords products in moderate to high yields (up to 96%) with excellent diastereoselecti...

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Detalles Bibliográficos
Autores principales: Zheng, Ya-Yun, Feng, Kai-Xiang, Xia, Ai-Bao, Liu, Jie, Tang, Cheng-Ke, Zhou, Zhan-Yu, Xu, Dan-Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062170/
https://www.ncbi.nlm.nih.gov/pubmed/35520709
http://dx.doi.org/10.1039/c9ra01665a
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author Zheng, Ya-Yun
Feng, Kai-Xiang
Xia, Ai-Bao
Liu, Jie
Tang, Cheng-Ke
Zhou, Zhan-Yu
Xu, Dan-Qian
author_facet Zheng, Ya-Yun
Feng, Kai-Xiang
Xia, Ai-Bao
Liu, Jie
Tang, Cheng-Ke
Zhou, Zhan-Yu
Xu, Dan-Qian
author_sort Zheng, Ya-Yun
collection PubMed
description A new and efficient one-pot strategy combining catalyst-free synthesis and iodine catalysis has been developed for the synthesis of dihydrofuropyrimidines and spirodihydrofuropyrimidine pyrazolones. This approach affords products in moderate to high yields (up to 96%) with excellent diastereoselectivities (up to >25 : 1 dr). The reaction is simple to carry out and is metal-free.
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spelling pubmed-90621702022-05-04 Merging catalyst-free synthesis and iodine catalysis: one-pot synthesis of dihydrofuropyrimidines and spirodihydrofuropyrimidine pyrazolones Zheng, Ya-Yun Feng, Kai-Xiang Xia, Ai-Bao Liu, Jie Tang, Cheng-Ke Zhou, Zhan-Yu Xu, Dan-Qian RSC Adv Chemistry A new and efficient one-pot strategy combining catalyst-free synthesis and iodine catalysis has been developed for the synthesis of dihydrofuropyrimidines and spirodihydrofuropyrimidine pyrazolones. This approach affords products in moderate to high yields (up to 96%) with excellent diastereoselectivities (up to >25 : 1 dr). The reaction is simple to carry out and is metal-free. The Royal Society of Chemistry 2019-03-27 /pmc/articles/PMC9062170/ /pubmed/35520709 http://dx.doi.org/10.1039/c9ra01665a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zheng, Ya-Yun
Feng, Kai-Xiang
Xia, Ai-Bao
Liu, Jie
Tang, Cheng-Ke
Zhou, Zhan-Yu
Xu, Dan-Qian
Merging catalyst-free synthesis and iodine catalysis: one-pot synthesis of dihydrofuropyrimidines and spirodihydrofuropyrimidine pyrazolones
title Merging catalyst-free synthesis and iodine catalysis: one-pot synthesis of dihydrofuropyrimidines and spirodihydrofuropyrimidine pyrazolones
title_full Merging catalyst-free synthesis and iodine catalysis: one-pot synthesis of dihydrofuropyrimidines and spirodihydrofuropyrimidine pyrazolones
title_fullStr Merging catalyst-free synthesis and iodine catalysis: one-pot synthesis of dihydrofuropyrimidines and spirodihydrofuropyrimidine pyrazolones
title_full_unstemmed Merging catalyst-free synthesis and iodine catalysis: one-pot synthesis of dihydrofuropyrimidines and spirodihydrofuropyrimidine pyrazolones
title_short Merging catalyst-free synthesis and iodine catalysis: one-pot synthesis of dihydrofuropyrimidines and spirodihydrofuropyrimidine pyrazolones
title_sort merging catalyst-free synthesis and iodine catalysis: one-pot synthesis of dihydrofuropyrimidines and spirodihydrofuropyrimidine pyrazolones
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062170/
https://www.ncbi.nlm.nih.gov/pubmed/35520709
http://dx.doi.org/10.1039/c9ra01665a
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