Microwave-Assisted Amination of a Chloropurine Derivative in the Synthesis of Acyclic Nucleoside Analogues
An efficient protocol for the amination of 6-chloropurine derivatives through nucleophilic aromatic substitution under microwave irradiation was developed and applied to the synthesis in two steps of a series of new acyclic nucleosides (acyclovir analogues) starting from commercially available compo...
Main Authors: | H.-G. Schmalz, A. Lanver |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2005-02-01
|
Series: | Molecules |
Subjects: | |
Online Access: | http://www.mdpi.com/1420-3049/10/2/508/ |
Similar Items
-
Microwave assisted synthesis of quinoxaline derivatives
by: Lucas K. Beagle, et al.
Published: (2023-12-01) -
Nucleophilic displacement reactions of 5′-derivatised nucleosides in a vibration ball mill
by: Olga Eguaogie, et al.
Published: (2017-01-01) -
Microwave-assisted synthesis of azepines via nucleophilic aromatic substitution
by: Božinović Nina, et al.
Published: (2016-01-01) -
Synthesis of some novel hydrazono acyclic nucleoside analogues
by: Mohammad N. Soltani Rad, et al.
Published: (2010-05-01) -
1,2,3-Triazoles as leaving groups: SNAr reactions of 2,6-bistriazolylpurines with O- and C-nucleophiles
by: Dace Cīrule, et al.
Published: (2021-02-01)