Date of Award
Spring 2026
Document Type
Open Access Thesis
Department
Chemistry and Biochemistry
First Advisor
Ken Shimizu
Abstract
An anionic cascade reaction comprising sequences of Michael and anti-Michael reactions has been identified as resulting in the formation of a novel spirolactam product. This novel spirolactam product was formed serendipitously during the attempted desilylation of a TMS-protected acetylenic amide.
Rights
© 2026, Oluebube Faith Ezenwafor
Recommended Citation
Ezenwafor, O. F.(2026). Formation of Spirolactams via Cascade Trimerization of Acetylenic Amides. (Master's thesis). Retrieved from https://scholarcommons.sc.edu/etd/8940