𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Stereoselective preparation of methyl (Z)-cinnamates by favorskii rearrangement

✍ Scribed by Thomas A Engler; Wolfgang Falter


Publisher
Elsevier Science
Year
1986
Tongue
French
Weight
137 KB
Volume
27
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Facile stereoselective syntheses of (E)-
✍ Hiroshi Sai; Hiroshi Ohmizu πŸ“‚ Article πŸ“… 1999 πŸ› Elsevier Science 🌐 French βš– 207 KB

Highly stereoselective syntheses of (EL)-and (Z)-cx-substituted cinnamates have been achieved by dehydration reaction of anti-and syn-~x-substituted-~-hydroxyphenylpropionates with EDC in good yields. This facile method has been applied to the stereoselective syntheses of (E)~ and (Z)-~-alkylidene-y

Preparation of 2,4,5-triarylimidazol-4-o
✍ Gonghao Lu; Akira Katoh; Zhiqiang Zhang; Zhizhi Hu; Peng Lei; Masaru Kimura πŸ“‚ Article πŸ“… 2010 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 720 KB

## Abstract magnified image Lophine hydroperoxides underwent base‐triggered 1,5‐phenyl migration in DMSO to afford imidazolones in high yields, instead of amidines with chemiluminescence (CL). The corresponding imidazolols were believed to intermediates and they were successfully obtained by treati