607716-80-3Relevant articles and documents
Dinucleotides of 4′-C-vinyl- and 5′-C-allylthymidine as substrates for ring-closing metathesis reactions
Kirchhoff, Claus,Nielsen, Poul
, p. 6475 - 6478 (2003)
Thymidine derivatives containing a 4′-C-vinyl group or a 5′-C-allyl group are synthesized and used as building blocks for three different dinucleotides. These are evaluated as substrates for ring-closing metathesis cyclisations, and a protected 5′-C-allyl
A cyclic dinucleotide with a four-carbon 5′-C-to-5′-C connection; Synthesis by RCM, NMR-examination and incorporation into secondary nucleic acid structures
Sharma, Pawan K.,Mikkelsen, Birgitte H.,Christensen, Mikkel S.,Nielsen, Katrine E.,Kirchhoff, Claus,Pedersen, Soren L.,Sorensen, Anders M.,stergaard, Kirsten,Petersen, Michael,Nielsen, Poul
, p. 2433 - 2445 (2008/03/11)
A 5′-C-allylthymidine derivative was prepared from thymidine by the application of a stereoselective allylation procedure and its 5′(S)-configuration was confirmed. From this nucleoside derivative, appropriately protected building blocks were prepared and
