Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 1, Issue 18, Pages 3154-3159Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b305782h
Keywords
-
Categories
Ask authors/readers for more resources
The rearrangement of 2-bromomethyl-2-methylmonothiomalonates to succinyl derivatives was found to take place in quantitative yields in the presence of one molar equivalent of Co(I) generated by the reduction of heptamethyl Co(II) yrinate perchlorate with NaBH4 or electrochemically. The chiral thiomalonate gave racemic succinate.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available
Share Paper
