Hydroformylation of allyl ethers. A study of the regioselectivity using rhodium catalysts
✍ Scribed by Nuria Ruiz; Alfonso Polo; Sergio Castillón; Carmen Claver
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 124 KB
- Volume
- 137
- Category
- Article
- ISSN
- 1381-1169
No coin nor oath required. For personal study only.
✦ Synopsis
The hydroformylation of different substituted allyl benzyl ethers is studied using the precursor catalytic system w Ž
influence of the phosphorus auxiliary ligands on the isomerizationrhydroformylation processes is analyzed. High yields and Ž . low regioselectivities are obtained in the hydroformylation of allyl benzyl ether 1 using both P O-o-t-BuC H and PPh .
6 4 3 3 4-Benzyloxy-3-methyl-butanal 8 and 4-benzyloxy-2-methyl-butanal 11 were obtained in good to excellent yields, starting from benzyl-2-metallyl ether 2 and benzyl-2-buthenyl ether 3, respectively.
📜 SIMILAR VOLUMES
## Abstract Here, we describe the successful application of novel glucofuranose‐derived 1,3‐diphosphites in the rhodium‐catalysed asymmetric hydroformylation of vinyl acetate, 2,5‐dihydrofuran and 2,3‐dihydrofuran. In the hydroformylation of vinyl acetate, total regioselectivity and high __ee__ (up