16369-01-0Relevant academic research and scientific papers
Functionalization of solid supports with N-unprotected deoxyribonucleosides
Wada, Takeshi,Mochizuki, Akira,Sato, Yuichi,Sekine, Mitsuo
, p. 5593 - 5596 (1998)
N-Unprotected deoxyribonucleotides were loaded to solid supports via a succinyl or an oxalyl linker. These solid supports were successfully used for oligonucleotide synthesis by the H-phosphonate method without N-protecting groups.
Synthesis, Enzymatic Stability And Physicochemical Properties Of Oligonucleotides Containing A N-Cyanoguanidine Linkage.
Pannecouque, C.,Vandendriessche, F.,Rozenski, J.,Janssen, G.,Busson, R.,et. al
, p. 7231 - 7246 (2007/10/02)
Nucleoside dimers with a N-cyanoguanidine linkage were synthesized and used as building blocks for oligonucleotide synthesis.Oligonucleotides composed of alternating phosphodiester and cyanoguanidine functions are still able to hybridize with a complementary natural oligodeoxynucleotide.
