2,2‐Difluoro‐1,3‐Dimethylimidazolidine in Deoxyfluorinaton Reactions and Other Conversions

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Autor principal: Douglas A. Klumpp
Formato: Artículo Open Access
Publicado: Wiley 2026
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author Douglas A. Klumpp
author_facet Douglas A. Klumpp
Douglas A. Klumpp
collection Wiley Open Access
contents 2,2‐Difluoro‐1,3‐Dimethylimidazolidine in Deoxyfluorinaton Reactions and Other Conversions Douglas A. Klumpp Israel Journal of Chemistry 2,2‐Difluoro‐1,3‐dimethylimidazolidine (DFI) is useful in deoxyfluorination reactions—converting alcohols, aldehydes, and carboxylic acids to the corresponding organofluorine products. This manuscript surveys the chemistry of this compound. 10.1002/ijch.70021 http://onlinelibrary.wiley.com/termsAndConditions#vor
doi_str_mv 10.1002/ijch.70021
format Artículo Open Access
id wiley_oa_10_1002_ijch_70021
institution Wiley Open Access
license_str_mv http://onlinelibrary.wiley.com/termsAndConditions#vor
publishDate 2026
publisher Wiley
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spellingShingle 2,2‐Difluoro‐1,3‐Dimethylimidazolidine in Deoxyfluorinaton Reactions and Other Conversions
Douglas A. Klumpp
Israel Journal of Chemistry
2,2‐Difluoro‐1,3‐Dimethylimidazolidine in Deoxyfluorinaton Reactions and Other Conversions Douglas A. Klumpp Israel Journal of Chemistry 2,2‐Difluoro‐1,3‐dimethylimidazolidine (DFI) is useful in deoxyfluorination reactions—converting alcohols, aldehydes, and carboxylic acids to the corresponding organofluorine products. This manuscript surveys the chemistry of this compound. 10.1002/ijch.70021 http://onlinelibrary.wiley.com/termsAndConditions#vor
title 2,2‐Difluoro‐1,3‐Dimethylimidazolidine in Deoxyfluorinaton Reactions and Other Conversions
topic Israel Journal of Chemistry
url https://onlinelibrary.wiley.com/doi/10.1002/ijch.70021