D. Mecerreyes, R.D. Miller, et al.
J Polym Sci Part A
Paper
Rearrangements initiated by trimethylsilyl iodide: the facile ring opening of some cyclobutanone derivatives
Abstract
The powerful electrophile trimethylsilyl iodide in the presence of certain catalysts rapidly and cleanly initiates the ring opening of a variety of cyclobutanone derivatives in a highly regioselective fashion yielding ultimately β-iodoketones. © 1980.
Related
Keith Lloyd, Matteo Cella, et al.
BMC Medical Informatics and Decision Making
David C. Spellmeyer, William C. Swope
Perspectives in Drug Discovery and Design
Aurélien Pélissier, Youcef Akrout, et al.
Cells