218601-09-3Relevant articles and documents
Participation of sulfur occurred during the Mitsunobu reaction: Synthesis of novel isodideoxythionucleosides
Jeong, Lak Shin,Yoo, Su Jeong,Moon, Hyung Ryong,Kim, Yun Ha,Chun, Moon Woo
, p. 3325 - 3326 (1998)
Novel isodideoxythionucleosides have been synthesized from our versatile intermediate, L-4-thioarabitol derivative 5 using the Mitsunobu reaction as a key step. It is found that the sulfur atom of the 4-thiofuranose derivative takes part in the Mitsunobu
A highly efficient synthesis of L-β-2′-deoxy-4′-thio-1′-purine nucleosides as potential antiviral agents
Kirn, Hea Ok,Jeong, Lak Shin,Sun Lee, Nan,Yoo, Soo Jeong,Moon, Hyung Ryong,Kirn, Kil Soo,Chun, Moon Woo
, p. 1327 - 1329 (2007/10/03)
L-β-2′-Deoxy-4′-thio-1′-purine nucleosides were synthesized efficiently utilizing the neighboring group effect of the 2-benzoyl-4-thiosugar acetate. The Royal Society of Chemistry 2000.
Ring contraction and rearrangement of 4-thiofuranose derivatives observed during dast fluorination in the synthesis of L-2'-'up'-fluoro-4'- thiothymidine
Jeong, Lak Shin,Moon, Hyung Ryong,Yoo, Su Jeong,Lee, Sun Nan,Chun, Moon Woo,Lim, Yoong-Ho
, p. 5201 - 5204 (2007/10/03)
Ring contraction and rearrangement of 4-thiofuranose derivatives were observed through the regioselective opening of the episulfonium ion formed during DAST fluorination in the synthesis of L-2'-'up'-fluoro-4'- thiothymidine.