Stereocontrolled Synthesis of Functionalized Azaheterocycles from Carbocycles through Oxidative Ring Opening/Reductive Ring Closing Protocols

Fluorine-containing organic scaffolds are of significant interest in medicinal chemistry. The incorporation of fluorine into biomolecules can lead to remarkable changes in their physical, chemical, and biological properties. There are already many drugs on the market, which contain at least one fluo...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Kiss Loránd
Lamiaa Ouchakour
Ábrahámi Renáta
Nonn Melinda
Dokumentumtípus: Cikk
Megjelent: 2020
Sorozat:CHEMICAL RECORD 20 No. 2
doi:10.1002/tcr.201900025

mtmt:30759804
Online Access:http://publicatio.bibl.u-szeged.hu/16695
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490 0 |a CHEMICAL RECORD  |v 20 No. 2 
520 3 |a Fluorine-containing organic scaffolds are of significant interest in medicinal chemistry. The incorporation of fluorine into biomolecules can lead to remarkable changes in their physical, chemical, and biological properties. There are already many drugs on the market, which contain at least one fluorine atom. Saturated functionalized azaheterocycles as bioactive substances have gained increasing attention in pharmaceutical chemistry. Due to the high biorelevance of organofluorine molecules and the importance of N-heterocyclic compounds, selective stereocontrolled procedures to the access of new fluorine-containing saturated N-heterocycles are considered to be a hot research topic. This account summarizes the synthesis of functionalized and fluorine-containing saturated azaheterocycles starting from functionalized cycloalkenes and based on oxidative ring cleavage of diol intermediates followed by ring expansion with reductive amination. 
700 0 1 |a Lamiaa Ouchakour  |e aut 
700 0 1 |a Ábrahámi Renáta  |e aut 
700 0 1 |a Nonn Melinda  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/16695/1/kissL_chemrec.pdf  |z Dokumentum-elérés