The ring-closing metathesis method is applied in the construction of conformationally
restricted bicyclic nucleosides. From diacetone-D-glucose, the unsaturated bicyclic …

The ring-closing metathesis reaction has been used in the synthesis of conformationally
restricted dinucleotides as well as a 3 '-nucleotide analogue. From bis-allylic nucleoside …

Full article: Bi- and Tricyclic Nucleoside Derivatives Restricted in S-Type Conformations and
Obtained by RCM-Reactions Skip to Main Content Taylor and Francis Online homepage Taylor …

A [4.3. 0] bicyclic nucleoside that contains an unsaturated hydroxylated 3′, 4′-trans
linkage has been efficiently synthesised. Thus, from diacetone-d-glucose as the starting …

This paper describes an efficient synthetic route for various types of novel carbocyclic
nucleosides. The required stereochemistry of the targeted nucleosides was successfully …

A New Synthetic Route to Nucleosides: Dissymmetric Construction of a Cyclopentene
System by Double [3,3]-Sigmatropic Rearrangement and Double Ring-Closing Metathesis …

Bis-, tris-, and tetrakisuracil-substituted 12-, 13-, 17-, and 21-membered macrocyclic
nucleoside analogues with polyether linkages, including C 2-symmetric molecules, have …

We have developed a route to the synthesis of new six-membered ring bicyclic nucleoside
analogues. The synthesis of 4′-C, 3′-O bicyclic thymidine analogues is presented as first …

An efficient synthetic route for preparing novel $4'{\alpha} $-C phenyl branched carbocyclic
nucleoside is described. The installation of phenyl group at the $4'$-position of carbocyclic …

Iridium (I)-catalyzed allylation of the enantiopure monoprotected copper (I) alkoxide,
generated from (S)-5a, with the enantiopure allylic carbonates (R)-9a, b has been …