Title
Reactions Of Β-Fluorovinamidinium Salt With Bifunctional Hetero Nucleophiles. A New Synthetic Route To Fluorinated Heterocycles
Abstract
β-Fluorovinamidinium salt (2), readily prepared fromN-(2, 3, 3-trifluoro-1-propenyl)trimethyl-ammonium iodide (1) and diethylamine, reacted with bifunctional hetero nucleophiles such as amidine and guanidine hydrochlorides in the presence of a base to afford regiospecifically monofluorinated pyrimidines4 in good yields. The one-pot procedure starting from1 was applicable for synthesizing heterocyclic compounds4 in almost comparable yields. © 1995 Elsevier Science Ltd.
Publication Date
2-27-1995
Publication Title
Tetrahedron Letters
Volume
36
Issue
9
Number of Pages
1527-1530
Document Type
Article
Personal Identifier
scopus
DOI Link
https://doi.org/10.1016/0040-4039(95)00076-O
Copyright Status
Unknown
Socpus ID
0028959333 (Scopus)
Source API URL
https://api.elsevier.com/content/abstract/scopus_id/0028959333
STARS Citation
Shi, Xifeng; Ishihara, Takashi; and Yamanaka, Hiroki, "Reactions Of Β-Fluorovinamidinium Salt With Bifunctional Hetero Nucleophiles. A New Synthetic Route To Fluorinated Heterocycles" (1995). Scopus Export 1990s. 2012.
https://stars.library.ucf.edu/scopus1990/2012