Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

Synthesis of an enantiomerically pure intermediate to (+)-thienamycin is presented: the pivotal reaction in this sequence is the highly diastereoselective Michael addition of a differentially protected lithium amide. © 1995.

Original publication

DOI

10.1016/0957-4166(95)00327-L

Type

Journal article

Journal

Tetrahedron: Asymmetry

Publication Date

01/01/1995

Volume

6

Pages

2507 - 2510