𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of Fused Heterocycles with a Benzazepinone Moiety via Intramolecular Heck Coupling.

✍ Scribed by Lionel Joucla; Aurelien Putey; Benoit Joseph


Publisher
John Wiley and Sons
Year
2006
Weight
23 KB
Volume
37
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Synthesis of (-)-herbertenediol and (aR,
✍ Ai-Min Zhang; Guo-Qiang Lin 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 575 KB

## Abstract Total enantioselective synthesis of the natural (‐)‐Herbertenediol (1) was accomplished in eleven steps with an overall yield of 15% starting from the 2‐methoxy‐4‐methyl‐phenol. The total synthesis features asymmetric intramolecular Heck reaction and Wolff‐Kishner‐Huang reduction. (a__R

Synthesis of C-nucleosides via coupling
✍ Masataka Yokoyama; Mitsuru Nomura; Takeshi Tanabe; Hideo Togo 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 487 KB

The direct coupling reaction of mribosyl fluoride with typical 7-excessive aromatic heterocycles such as furan, thiophene, pyrrole, benzofuran, benzothiophene, and indole and their trimethybilyl derivatives was performed in the presence of boron trifluoride to afford the corresponding C-nucleosides

2-Butyl-5-chloro-3H-imidazole-4-carbalde
✍ S. L. Gaonkar; K. M. Lokanatha Rai 📂 Article 📅 2010 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 81 KB 👁 1 views

## Abstract magnified image The title compound 2‐butyl‐5‐chloro‐3__H__‐imidazole‐4‐carbaldehyde was transformed into tricyclic heterocycles by substituting the chlorine atom by an unsaturated thiolate or alkoxide and then converting aldehyde function into 1,3‐dipole. Chloramine‐T was used as an ef