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Easily accessible non-aromatic heterocycles with handles: 4-bromo-2,3-dihydrofurans from 1,2-dibromohomoallylic alcohols

The first general preparation of 4-bromo-2,3-dihydrofurans is reported. These non-aromatic heterocycles containing a useful coupling handle are accessed via Cu-catalyzed intramolecular cyclization of 1,2-dibromohomoallylic alcohols, which are themselves available in just two steps from aromatic and...

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Autores principales: An, Jason, Intano, Jose, Richard, Alissa, Kim, Taehyun, Gascón, José A., Howell, Amy R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8336482/
https://www.ncbi.nlm.nih.gov/pubmed/34377420
http://dx.doi.org/10.1039/d1sc01013a
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author An, Jason
Intano, Jose
Richard, Alissa
Kim, Taehyun
Gascón, José A.
Howell, Amy R.
author_facet An, Jason
Intano, Jose
Richard, Alissa
Kim, Taehyun
Gascón, José A.
Howell, Amy R.
author_sort An, Jason
collection PubMed
description The first general preparation of 4-bromo-2,3-dihydrofurans is reported. These non-aromatic heterocycles containing a useful coupling handle are accessed via Cu-catalyzed intramolecular cyclization of 1,2-dibromohomoallylic alcohols, which are themselves available in just two steps from aromatic and aliphatic aldehydes and ketones. Molecular dynamics simulations using the simple substrates and key geometric parameters provide a rationale for the selectivities observed. The synthetic utility of the 4-bromodihydrofurans is also demonstrated.
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spelling pubmed-83364822021-08-09 Easily accessible non-aromatic heterocycles with handles: 4-bromo-2,3-dihydrofurans from 1,2-dibromohomoallylic alcohols An, Jason Intano, Jose Richard, Alissa Kim, Taehyun Gascón, José A. Howell, Amy R. Chem Sci Chemistry The first general preparation of 4-bromo-2,3-dihydrofurans is reported. These non-aromatic heterocycles containing a useful coupling handle are accessed via Cu-catalyzed intramolecular cyclization of 1,2-dibromohomoallylic alcohols, which are themselves available in just two steps from aromatic and aliphatic aldehydes and ketones. Molecular dynamics simulations using the simple substrates and key geometric parameters provide a rationale for the selectivities observed. The synthetic utility of the 4-bromodihydrofurans is also demonstrated. The Royal Society of Chemistry 2021-06-29 /pmc/articles/PMC8336482/ /pubmed/34377420 http://dx.doi.org/10.1039/d1sc01013a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
An, Jason
Intano, Jose
Richard, Alissa
Kim, Taehyun
Gascón, José A.
Howell, Amy R.
Easily accessible non-aromatic heterocycles with handles: 4-bromo-2,3-dihydrofurans from 1,2-dibromohomoallylic alcohols
title Easily accessible non-aromatic heterocycles with handles: 4-bromo-2,3-dihydrofurans from 1,2-dibromohomoallylic alcohols
title_full Easily accessible non-aromatic heterocycles with handles: 4-bromo-2,3-dihydrofurans from 1,2-dibromohomoallylic alcohols
title_fullStr Easily accessible non-aromatic heterocycles with handles: 4-bromo-2,3-dihydrofurans from 1,2-dibromohomoallylic alcohols
title_full_unstemmed Easily accessible non-aromatic heterocycles with handles: 4-bromo-2,3-dihydrofurans from 1,2-dibromohomoallylic alcohols
title_short Easily accessible non-aromatic heterocycles with handles: 4-bromo-2,3-dihydrofurans from 1,2-dibromohomoallylic alcohols
title_sort easily accessible non-aromatic heterocycles with handles: 4-bromo-2,3-dihydrofurans from 1,2-dibromohomoallylic alcohols
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8336482/
https://www.ncbi.nlm.nih.gov/pubmed/34377420
http://dx.doi.org/10.1039/d1sc01013a
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