𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A Reexamination of the Retro-fries Rearrangement of Some o-Hydroxyketones

✍ Scribed by Robert Martin; Jean Ronald Lafrance; Pierre Demerseman

Publisher
Wiley (John Wiley & Sons)
Year
2010
Weight
583 KB
Volume
100
Category
Article
ISSN
0037-9646

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: The Acetyl Derivati
ChemInform Abstract: The Acetyl Derivative of a Novel Fries Rearrangement Product.
✍ S. C. JAIN; S. TALWAR; R. KUMAR; B. R. BABU; W. ERRINGTON πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 25 KB πŸ‘ 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

The Fries rearrangement of p-tolyl and o
The Fries rearrangement of p-tolyl and o-tolyl acetate catalysed by aluminium chloride
✍ N. M. Cullinane; B. F. R. Edwards; V. V. Bailey-Wood πŸ“‚ Article πŸ“… 2010 πŸ› Elsevier Science 🌐 English βš– 280 KB

## Abstract The rearrangement of __p__‐tolyl acetate in nitrobenzene solution catalysed by aluminium chloride gives the __o__‐hydroxyketone only as rearrangement product. __o__‐Tolyl acetate under the same treatment yields mainly the __para__‐substituted hydroxyketone together with a small amount o

A versatile tandem retro-[1,4]-Brook rea
A versatile tandem retro-[1,4]-Brook rearrangement-condensation reaction of o-bromoacetophenone silyl enol ethers
✍ Bogdan M. Comanita; Simon Woo; Alex G. Fallis πŸ“‚ Article πŸ“… 1999 πŸ› Elsevier Science 🌐 French βš– 246 KB

The retro-[1,4]-Brook rearrangement (also referred to as the West or silyl-Wittig rearrangement) has been employed with acetophenone silyl enol ethers to allow regiospecific migration of the silicon from oxygen to the ortho position of the aromatic ring. The enolate that results from this process ma