𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Nonafluorobutanesulfonyl Azide: A Shelf-Stable Diazo Transfer Reagent for the Synthesis of Azides from Primary Amines.

✍ Scribed by Jose Ramon Suarez; Beatriz Trastoy; M. Eugenia Perez-Ojeda; Ruben Marin-Barrios; Jose Luis Chiara

Publisher
John Wiley and Sons
Year
2011
Weight
46 KB
Volume
42
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Nonafluorobutanesulfonyl Azide: A Shelf-
Nonafluorobutanesulfonyl Azide: A Shelf-Stable Diazo Transfer Reagent for the Synthesis of Azides from Primary Amines
✍ José Ramón Suárez; Beatriz Trastoy; M. Eugenia Pérez-Ojeda; Rubén Marín-Barrios; 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 178 KB 👁 2 views

## Abstract Nonafluorobutanesulfonyl azide is an efficient, shelf‐stable and cost‐effective diazo transfer reagent for the synthesis of azides from primary amines. The reagent can also be successfully applied to the one‐pot regioselective synthesis of 1,2,3‐triazoles from primary amines by a sequen

A Safe and Convenient Method for the Pre
A Safe and Convenient Method for the Preparation of Triflyl Azide, and Its Use in Diazo Transfer Reactions to Primary Amines.
✍ Alexander Titz; Zorana Radic; Oliver Schwardt; Beat Ernst 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 18 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

ChemInform Abstract: Iodotrimethylsilane
ChemInform Abstract: Iodotrimethylsilane: A Mild and Efficient Reagent for the Reduction of Azides to Amines.
✍ A. KAMAL; N. V. RAO; E. LAXMAN 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 1 views

Iodotrimethylsilane: A Mild and Efficient Reagent for the Reduction of Azides to Amines. -An efficient and chemoselective protocol for the reduction of azides using in situ prepared iodotrimethylsilane as a reducing agent is reported. The corresponding amines are formed in excellent yields. -