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Highly efficient catalytic asymmetric acylation of meso-1,2-diols with benzoyl chloride in the presence of a chirai diamine combined with Et3N

✍ 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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✦ 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.


πŸ“œ SIMILAR VOLUMES


Asymmetric acylation of meso-diols with
✍ Takeshi Oriyama; Keisuke Imai; Takeshi Hosoya; Tomohumi Sano πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 French βš– 222 KB

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.

ChemInform Abstract: Catalytic Asymmetri
✍ Tohru Yamada πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 22 KB πŸ‘ 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v