Tetrahedron Letters

Paper

01 Jan 1980

Rearrangements initiated by trimethylsilyl iodide: the facile ring opening of some cyclobutanone derivatives

View publication

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

Paper

Modeling and measurement of the spontaneous mutation rate in mammalian cells

Toby G. Rossman, Ekaterina I. Goncharova, et al.

Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis

Paper

Ring-opening polymerization of 6-hydroxynon-8-enoic acid lactone: Novel biodegradable copolymers containing allyl pendent groups

D. Mecerreyes, R.D. Miller, et al.

J Polym Sci Part A

Paper

Clinical application of machine learning and computer vision to indocyanine green quantification for dynamic intraoperative tissue characterisation: how to do it

Niall P. Hardy, Pol Mac Aonghusa, et al.

Surgical Endoscopy

Paper

Inferring Parameters of Pyramidal Neuron Excitability in Mouse Models of Alzheimer’s Disease Using Biophysical Modeling and Deep Learning

Soheil Saghafi, Timothy Rumbell, et al.

Bulletin of Mathematical Biology

View all publications