𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Tunable Phosphine-Mediated Domino Reaction: Selective Synthesis of 2,3-Dihydrofurans and Biaryls

✍ Scribed by Xie, Peizhong; Li, Erqing; Zheng, Jie; Li, Xin; Huang, You; Chen, Ruyu

Book ID
118750985
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
345 KB
Volume
355
Category
Article
ISSN
1615-4150

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Tunable Carbonyl Yl
ChemInform Abstract: Tunable Carbonyl Ylide Reactions: Selective Synthesis of Dihydrofurans and Dihydrobenzoxepines.
✍ Jiao-Long Zhou; Yong Liang; Chao Deng; Haolai Zhou; Zheng Wang; Xiu-Li Sun; Jun- πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons βš– 35 KB

## Abstract DFT calculations show, that the bulkiness of the ligand controls the reaction between α‐benzylidene‐β‐dicarbonyl compounds (I) and diazoacetate (II) to give either the five‐ or seven‐membered products (III)/(V) or (VI)/(VII).

Efficient and mild synthesis of function
Efficient and mild synthesis of functionalized 2,3-dihydrofuran derivatives via domino reaction in water
✍ Jian-Wu Xie; Ping Li; Ting Wang; Fei-Ting Zhou πŸ“‚ Article πŸ“… 2011 πŸ› Elsevier Science 🌐 French βš– 640 KB

An efficient and mild method for the synthesis of functionalized tricyclic 2,3-dihydrofurans, bicyclic 2,3dihydrofurans, and other tetrasubstituted 2,3-dihydrofurans by domino reaction of 1,3-dicarbonyl compounds and a-bromonitroalkenes with a large substrate scope and excellent diastereoselectivity