The configurational stability of enantiopure chiral (2, 4, 6-triisopropylbenzoyl) oxy-[D1] methyllithium generated by a tin− lithium exchange was tested on the macroscopic time scale, employing trapping experiments with benzaldehyde. It was found to be configurationally stable for minutes at− 78° C and to be an appropriate substitute for the carbamoyloxy-substituted analogue in terms of cleavage. Its addition to several ...
![S-methyl O-[1-phenyl-2-(2,4,6-triisopropylbenzoyloxy)ethyl] dithiocarbonate Structure](https://image.chemsrc.com/caspic/192/1133931-92-6.png)
