Highly efficient catalytic asymmetric acylation of meso-1,2-diols with benzoyl chloride in the presence of a chirai diamine combined with Et3N
β Scribed by Takeshi Oriyama; Keisuke Imai; Tomohumi Sano; Takeshi Hosoya
- Book ID
- 104259171
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 209 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Catalytic asymmetric acylation of meso-l,2-ciols has been successfully performed by the reaction with benzoyl chlarid~ in the presence of 0.5 mol% of Β’hiral ~amine derived from (S)-proline combined with a stoichiom etric amount of triethylamine to give the corresponding monobenzoate with good to excellent enantioselecti vities.
π SIMILAR VOLUMES
Nonmzymatic desymmetdzation ofcis-l,2-cyclohexmlediol by the asymmetric acylation with achiral ben~oyl chloride in the presence ofa ehiral dimnine derived from (S)-proline took place to give monobenzoate in high optical yield.
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