Abstract
In contrast with keto diester ( R)- 10a bearing a methyl ester group at the quaternary carbon center, the benzyl ester analogue ( R)- 10a partially racemized during workup, thereby revealing that the nature of the ester group at the quaternary carbon center has a critical role in the rate of racemization of such Michael adducts.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Paper version not known
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
