Synthesis of 2′-Fluorinated Northern Methanocarbacyclic (2′-F-NMC) Nucleosides and Their Incorporation Into Oligonucleotides

Abstract

This article describes chemical synthesis of 2′-fluorinated Northern methanocarbacyclic (2′-F-NMC) nucleosides and phosphoramidites, based on a bicyclo[3.1.0]hexane scaffold bearing all four natural nucleobases (U, C, A, and G), and their incorporation into oligonucleotides by solid-supported synthesis. This synthesis starts from commercially available cyclopent-2-en-1-one to obtain the fluorinated carbocyclic pseudosugar intermediate (S.13), which can be converted to the uridine intermediate by condensation with isocyanate, followed by cyclization, and to adenine and guanine precursors by microwave-assisted reactions. All four 2′-F-NMC phosphoramidites are synthesized from S.13 in a convergent approach, and the monomers are used for synthesis of 2′-F-NMC-modified oligonucleotides. © 2020 by John Wiley & Sons, Inc.

Basic Protocol 1: Preparation of fluorinated carbocyclic pseudosugar intermediate

Basic Protocol 2: Preparation of 2′-F-NMC uridine and cytidine phosphoramidites

Basic Protocol 3: Preparation of 2′-F-NMC adenosine phosphoramidite

Basic Protocol 4: Preparation of 2′-F-NMC guanosine phosphoramidite

Basic Protocol 5: Synthesis of oligonucleotides containing 2ʹ-F-NMC