Previous investigators of the co-oxidation reaction of indene and thiophenol claim (1) the formation of only trace amounts (0.23%) of the cis --hydroxy sulfoxide, and this result is
Direct evidence for equilibration in a reformatsky reaction and for dependence of its stereoselectivity on electronic substituent effect
✍ Scribed by A. Balsamo; P.L. Barili; P. Crotti; M. Ferretti; B. Macchia; F. Macchia
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- French
- Weight
- 194 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Although the Reformatsky reaction' has been extensively investigated, there are still many unoertain points about its mechanism,2 and particularly on whether the formation of diastereoisomeric hydroxyesters is under kinetic or thermodynamic control, *1~2a~b~3 indirect evidence in favor or against equilibration of these products has been reported.3 We have now obtained direct evidence for an initial kinetic control and for a slower equilibration of the diastereoisomers in the reaction medium.
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