## Abstract For Abstract see ChemInform Abstract in Full Text.
Stereo- and regioselective synthesis of 1,3-diaryl-3-chloro-1-propanols via the reaction of aryl aldehydes with styrene and (E)-β-methylstyrene
✍ Scribed by George W. Kabalka; Zhongzhi Wu; Yuhong Ju
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 100 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Reactions of aryl aldehydes with styrene and (E)-b-methylstyrene in the presence of phenylboron dichloride regioselectively generate 1,3-diaryl-3-chloro-1-propanols and 1,3-diaryl-3-chloro-2-methyl-1-propanols in good to excellent yields with high stereoselectivity.
📜 SIMILAR VOLUMES
The reaction of dibenzylideneacetones or E,E-cinnamylidene-acetophenones and hydrazine hydrate provided 1-propionyl derivatives of 5-aryl-3-styryl-2-pyrazolines and 3-aryl-5-styryl-2-pyrazolines. These unsaturated ketones afforded 1-(2-carboxyphenyl) or 1-(4-carboxyphenyl) 5-aryl-3-styryl-2-pyrazoli
An efficient ZrCl 4 catalyzed ortho-hydroxyalkylation of phenols with aldehydes promoted by 3,5-bis (trifluoromethyl)phenyl boronic acid, leading to the formation of 2-aryl-1,3,2-aryldioxaborins was investigated and optimized. The reaction afforded the desired aryldioxaborins in good to excellent yi