𝔖 Bobbio Scriptorium
✦   LIBER   ✦

2′(3)′-O-l-(O-methyl-3-phenyllactyl) adenosine A potential analog of 2′(3′)-O-aminoacyl ribonucleosides

✍ Scribed by Jiří Žemlička; James Owens


Book ID
115746320
Publisher
Elsevier Science
Year
1976
Weight
330 KB
Volume
442
Category
Article
ISSN
0005-2787

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Synthesis of 2′(3′)-O-aminoacyl derivati
✍ J. Žemlička; S. Chládek 📂 Article 📅 1965 🏛 Elsevier Science 🌐 French ⚖ 290 KB

The eeterificatlon of the hydroxyllc function in position8 2' or 3' of the terminal adenoslne unit of the soluble (tran8fer) ribonucleic acid by an emin acid repreeent8 an important step in the biosynth88is of proteins (1). Although no non-enzymatic method8 for the attechaent Of an miuOaCy1 residue

An expeditious synthesis of 3′-α-carboxy
✍ Peter von Matt; Thomas Lochmann; Rudolf Kesselring; Karl-Heinz Altmann 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 287 KB

3'-a-Carboxymethyl-2"O-methyl ribonucleosides, which are important building blocks for the construction of high affinity amide modified antisense oligonucleotides, have been synthesized from the corresponding 2'-O-methyl ribonucleosides via catalytic hydrogenation of their 3'-deoxy 3'-methoxycarbony

Synthesis of 2,3-O-isopropylidene- and 3
✍ Masanori Yamaura; Tsuneji Suzuki; Yuji Tagami; Hironobu Hashimoto; Juji Yoshimur 📂 Article 📅 1988 🏛 Elsevier Science 🌐 English ⚖ 438 KB

2-C-Methylglyceraldehyde derivatives are among the simplest branchedchain chiral synthons and both the (R)-enantiomer and the (S)-enantiomer 'To whom correspondence should be addressed. \*The temperature reported in ref. 4 must be revised.