94697-73-1Relevant academic research and scientific papers
Diastereoselective Aldol Reactions of β-Silylenolates: A Formal Synthesis of Thienamicin
Fleming, Ian,Kilburn, Jeremy D.
, p. 1198 - 1199 (1986)
The lithium enolate (1) of benzyl β-phenyldimethylsilylbutanoate reacts with β-phenyldimethylsilylpropionaldehyde (2) to give, with high diastereoselectivity, the aldol product (3), which is converted into the β-lactam (7), a known precursor of thienamyci
