𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Efficient and β-Stereoselective Synthesis of 4(5)-(β-D-Ribofuranosyl)- and 4(5)-(2-Deoxyribofuranosyl)imidazoles.

✍ Scribed by S. HARUSAWA; Y. MURAI; H. MORIYAMA; T. IMAZU; H. OHISHI; R. YONEDA; T. KURIHARA

Book ID
112039601
Publisher
John Wiley and Sons
Year
2010
Weight
36 KB
Volume
27
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Syntheses of [2-2H]-5-ethynyl-1-(β-D-rib
Syntheses of [2-2H]-5-ethynyl-1-(β-D-ribofuranosyl)imidazole-4-carboxamide and 5-ethynyl-1-([5-3H]-β-D-ribofuranosyl)imidazole-4-carboxamide (EICAR)
✍ Noriaki Minakawa; Akira Matsuda; Zuping Xia; Leonard I. Wiebe; Edward E. Knaus 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 French ⚖ 654 KB

Metallation of 5-ethynyl-1-(2,3,5-tri-O-terf-butyldimethylsilyl-~-~-ribof~anosyl)imidazole-4-carboxamide (1) using n-BuLi, deuteration with deuterium oxide and removal of the fertbutyldimethylsilyl protecting groups using tetrabutylammonium fluroide yielded [2-'H]-5ethynyl-1 -(~-D-ribofi1ranosyl)imi

ChemInform Abstract: Synthesis of 5-Hydr
ChemInform Abstract: Synthesis of 5-Hydroxy-2-(β-D-ribofuranosyl)pyran-4-one from a Pyranulose Glycoside.
✍ Shigeyuki Kanazawa; Souhei Mizuno; Rie Yamauchi; Natsu Nishimura; Isamu Maeba 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views

Synthesis of 5-Hydroxy-2-(β-D-ribofuranosyl)pyran-4-one from a Pyranulose Glycoside. -The title compound (VI) is synthesized from the pyranulose glycoside (I) by bromination, acetylation with Ac 2 O, and final deprotection with ammonia. -(KANAZAWA, SHIGEYUKI; MIZUNO,