129285-58-1Relevant academic research and scientific papers
Nucleosides. IX. Synthesis of Purine N3,5′ -Cyclonucleosides and N3,5′-Cyclo-2′,3′ -seconucleosides via Mitsunobu Reaction as TIBO-like Derivativest
Chen, Grace Shiahuy,Chen, Chien-Shu,Chien, Tun-Cheng,Yeh, Jun-Yen,Kuo, Chia-Chi,Talekar, Rahul Subhash,Chern, Ji-Wang
, p. 347 - 359 (2004)
The Mitsunobu reaction was applied to prepare, in one step, purine N 3,5′-cyclonucleosides 10a-d. A subsequent ring opening in the ribose moiety of the resultant N3,5′-nucleosides by sodium periodate led to the corresponding N3
Nucleosides XII.1 synthesis of 5′-modified isoguanosines and reinvestigation of 5′-deoxy-N3,5′-cycloisoguanosine
Chien, Tun-Cheng,Kuo, Chia-Chi,Chen, Chien-Shu,Chern, Ji-Wang
, p. 1401 - 1406 (2007/10/03)
Isoguanosine (3) underwent a coupling reaction with diaryl disulfides in the presence of tri-n-butylphosphine when its 6-amino group was protected by N,N-dimethylaminomethylidene. The synthesis of 5′-deoxy-N 3,5′-cycloisoguanosine (6) and its 2
