𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of novel derivatives of closo-dodecaborate anion with azido group at the terminal position of the spacer

✍ Scribed by Anna V. Orlova; Nikolay N. Kondakov; Boris G. Kimel; Leonid O. Kononov; Elena G. Kononova; Igor B. Sivaev; Vladimir I. Bregadze


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
101 KB
Volume
21
Category
Article
ISSN
0268-2605

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Two novel azido‐derivatives of closo‐dodecaborate anion with hydrophobic and hydrophilic spacers were prepared by reaction of tetrabutylammonium azide with cyclic oxonium derivatives of the closo‐dodecaborate anion. The compounds prepared can be regarded as precursors of derivatives of closo‐dodecaborate anion with amino group at the terminal position of a spacer or as building blocks for ‘click chemistry’, which are useful for preparation of various conjugates with targeting molecules. A concentration dependence of the ^11^B NMR spectra of functionalized derivatives of closo‐dodecaborate anion was discovered, which is of great importance for analytical purposes. Copyright © 2006 John Wiley & Sons, Ltd.


📜 SIMILAR VOLUMES


ChemInform Abstract: Synthesis of Novel
✍ N. SAITO; M. TANITSU; T. BETSUI; R. SUZUKI; A. KUBO 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 40 KB

Synthesis of Novel Octahydro-1,5-imino-3-benzazocin-4,7,10-trione Derivatives Having a Methyl Group at the C-2 Position as ABC Ring Models of Saframycins. -Simple and efficient syntheses of (Z)-3-benzylidenepiperazinedione ( VII) in both racemic and optically active forms are described. Compound (V