OXIDATIVE TRANSFORMATIONS OF NUCLEOSIDE FLUORENEMETHYL H-PHOSPHONOSELENOATE DIESTERS
Author:
Affiliation:
1. a Department of Organic Chemistry, Arrhenius Laboratory , Stockholm University , Stockholm, Sweden
2. b Institute of Bioorganic Chemistry, Polish Academy of Sciences , Poznan, Poland
Publisher
Informa UK Limited
Subject
Genetics,Molecular Medicine,Biochemistry,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1081/NCN-200060173
Reference4 articles.
1. 9-Fluorenemethyl H-Phosphonoselenoate—A Versatile Reagent for Transferring an H-Phosphonoselenoate Group
2. Studies on the Oxidation of Nucleoside Hydrogenphosphonates
3. 9-Fluorenemethyl H-phosphonothioate, a versatile reagent for the preparation of H-phosphonothioate, phosphorothioate, and phosphorodithioate monoesters
4. Nucleoside H-phosphonates. 14. Synthesis of nucleoside phosphoroselenoates and phosphorothioselenoates via stereospecific selenization of the corresponding H-phosphonate and H-phosphonothioate diesters with the aid of new selenium-transfer reagent, 3H-1,2-benzothiaselenol-3-one
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1. Solid-phase synthesis and structural characterisation of phosphoroselenolate-modified DNA: a backbone analogue which does not impose conformational bias and facilitates SAD X-ray crystallography;Chemical Science;2019
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