𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of a new class of acyclic 2′,5′- and 3′,5′-oligonucleotide analogs based on 9-[1,5-dihydroxy-4(S)-hydroxymethyl-3-oxapent-2(R)-yl]-adenine

✍ Scribed by Sergey N. Mikhailov; Wolfgang Pfleiderer

Publisher
Elsevier Science
Year
1985
Tongue
French
Weight
194 KB
Volume
26
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis

The acyclic analogs of 2',5'-and 3',5'-oligoadenylates possessing all functional groups of the natural compounds were prepared on the basis of "oxydized-reduced" adenosine.

📜 SIMILAR VOLUMES

Synthesis of a carba-sugar analog of tre
Synthesis of a carba-sugar analog of trehalosamine, [(1S)-(1,2,43,5)-2-amino-3,4-dihydroxy-5-hydroxymethyl-1-cyclohexyl] α-d-glucopyranoside, and a revised synthesis of its β anomer
✍ Seiichiro Ogawa; Kenji Nishi; Yasushi Shibata 📂 Article 📅 1990 🏛 Elsevier Science 🌐 English ⚖ 760 KB

Synthesis of a carba-sugar analog of trehalosamine, W9-(l2,4/3,W -amino-3,4-dihydroxy+hydroxymethyl-lcyclohexyl] a-D-glucopyranoside, and a revised synthesis of its j3 anomer\*

Synthesis and structures of a new class
Synthesis and structures of a new class of calixarene analogs derived from 5-t-butyltetrahydro-1,3,5-triazine-2(1H)one.
✍ Paritosh R. Dave; Gerald Doyle; Theodore Axenrod; Hamid Yazdekhasti; Herman L. A 📂 Article 📅 1992 🏛 Elsevier Science 🌐 French ⚖ 281 KB

## Representative members of a novel class of calixarene analogs derived from 5t-butyltetrahydro-1,3,5-triazine-2(1 H)one 1 have been synthesized and their structures and conformations investigated by X-ray crystallography and NMR spectroscopy.