Et3B–Pd-promoted allylation of benzaldehyde with allylic alcohols
✍ Scribed by Masanari Kimura; Tatsuya Tomizawa; Yoshikazu Horino; Shuji Tanaka; Yoshinao Tamaru
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 134 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
In the presence of Pd(OAc) 2 (0.05 equiv.) and PPh 3 (0.1 equiv.), triethylborane promotes a variety of allyl alcohols to undergo allylation of benzaldehyde to provide homoallyl alcohols in good yield.
📜 SIMILAR VOLUMES
Triethylborane promotes the Pd-catalyzed selective C-diallylation of o-hydroxyacetophenone and C-monoallylation of o-hydroxypropiophenone with a variety of ally alcohols. The reaction proceeds smoothly at 25-50°C and provides the allylation products in excellent yields.
## Abstract The combinations promote the reaction of cyclic hemiacetals with primary amines to generate cyclic hemiacetals which are in equilibrium with ω‐hydroxyimines.