194023-52-4Relevant articles and documents
Two convergent approaches toward novel carbocyclic C-nucleosides
Nencka, Radim,Sala, Michal,Dejmek, Milan,Drainsky, Martin,Holy, Antonin,Hebabecky, Hubert
scheme or table, p. 4119 - 4130 (2011/02/22)
Two convergent methodologies for construction of novel carbocyclic C-nucleosides allowing the syntheses of derivatives with uracil heterobase substituted at the position C-5 as well as C-6 were developed. The crucial step of the first methodology was the
Novel non-nucleosidic phosphoramidites for oligonucleotide modification and labeling
Su, Sheng-Hui,Iyer, Rajkumar S.,Aggarwal, Sunil K.,Kalra, Krishan L.
, p. 1639 - 1644 (2007/10/03)
A series of novel labeled phosphoramidites and CPG supports 1a-f with a new non-nucleosidic backbone based upon cyclohexyl-4-amino-1,1-dimethanol have been synthesized. These reagents have been used to label oligonucleotides with biotin and fluorescein at the 5'-, the 3'-, and internal positions.