Black Light Induced Radical Cyclization Approach to Cyclonucleosides: An Independent Approach

Author(s): Victoria T. Perchyonok

Journal Name: Letters in Organic Chemistry

Volume 8 , Issue 5 , 2011

Become EABM
Become Reviewer
Call for Editor


The paper highlights an efficient methodology based on consecutive radical reaction for the preparation of cyclonucleoside derivatives. The reactions were performed in organic and aqueous media, using common and efficient free radical hydrogen donors in the range of innovative and conventional initiation conditions to afford good to excellent yields of corresponding cyclonucleosides. The mechanistic aspects of the transformations are also addressed.

Keywords: Cyclo-nucleosides, black light, aqueous media, free radical reactions, dihydrothymidine, deoxyribose, chromatographic, diastereoisomers, oligonucleotides, cyclopyrimidine

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2011
Page: [337 - 340]
Pages: 4
DOI: 10.2174/157017811795685108
Price: $65

Article Metrics

PDF: 10