𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Reactions of Isocyanides and Pyridinium Triflates − A Simple and Efficient Route to Imidazopyridinium Derivatives

✍ Scribed by Jean-Claude Berthet; Martine Nierlich; Michel Ephritikhine


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
236 KB
Volume
2002
Category
Article
ISSN
1434-193X

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


ChemInform Abstract: A Simple and Effici
✍ L. CARRILLO; D. BADIA; E. DOMINGUEZ; J. L. VICARIO; I. TELLITU 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views

A Simple and Efficient Synthetic Route to Chiral Isopavines. Synthesis of (-)-O-Methylthalisopavine and (-)-Amurensinine. -The key steps in the synthesis of the title compounds (VIII) are stereoselective addition of the Grignard reagent (II) to the imines (I) and a novel one-pot double-intramolecul

ChemInform Abstract: Stille and Suzuki C
✍ C. W. HOLZAPFEL; C. DWYER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 38 KB 👁 1 views

Stille and Suzuki Cross Coupling Reactions of o-Nitrophenyl Triflates: A Versatile Route to a Variety of Heterocycles. -The cross coupling reaction of arylboron or arylstannane substrates with selected o-nitrophenyl triflates gives comparable yields of 2-nitrobiaryls which provide ready access to a