3′-C-phosphonates as nucleotides analogues synthesis starting from original C-phosphonosugars (in ribo- and deoxyribo- series)
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference36 articles.
1. Phosphonates as analogues of natural phosphates
2. Analogs of Nucleotides. II. Phosphonate Esters of Ribose and Glucopyranosyl Purine Derivatives1
3. The Synthesis of Nucleoside and Nucleotide Analogs Derived from Uridine*
4. Nucleoside Phosphonic Acids. I. The Synthesis of 5'-Deoxyuridine 5'-Phosphonic Acids and Derivatives*
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1. Application of DAST mediated reactions in transformations of α-hydroxyphosphonates derived from O-isopropylidene-protected carbohydrate derivatives;Phosphorus, Sulfur, and Silicon and the Related Elements;2017-05-25
2. Synthesis of Non-racemic α-Hydroxyphosphonates via Asymmetric Phospho‐Aldol Reaction;Phosphorus Chemistry II;2014
3. Stereoselective Methods for Carbon-Phosphorus (CP) Bond Formation;Stereoselective Synthesis of Drugs and Natural Products;2013-10-01
4. The Barton-McCombie Reaction;Organic Reactions;2012-01-25
5. ChemInform Abstract: 3′-C-Phosphonates as Nucleotide Analogues. Synthesis Starting from Original C-Phosphonosugars (in Ribo- and Deoxyribo-Series).;ChemInform;2010-08-18
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