𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The oxy-cope rearrangement of 1,2-divinylcyclohexanol: a novel synthesis of 5-cyclodecen-1-one

✍ Scribed by Elliot N. Marvell; William Whalley

Book ID
107858084
Publisher
Elsevier Science
Year
1970
Tongue
French
Weight
152 KB
Volume
11
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Influence of the stereochemistry on the
Influence of the stereochemistry on the 1,2-dialkenylcyclobutanols behaviour : oxy-cope versus retro-ene rearrangements
✍ J.P. Barnier; J. Ollivier; J. Salaun πŸ“‚ Article πŸ“… 1989 πŸ› Elsevier Science 🌐 French βš– 296 KB

From cyclobutanones Sa-j,ten 1,2-divinylcyclobutanot la-j were prepared. A stereochemical effect was clearly evidenced : while trans 1,2-divinylcyclobutanols underwent a retro-ene ring opening, the cis isomers underwent an oxy-Cope ring enlargement. It is well known that cis 1,2-divinylcyclobutanes

ChemInform Abstract: Oxy-Cope Rearrangem
ChemInform Abstract: Oxy-Cope Rearrangement of Bicyclo[3.2.0]heptenones. Synthesis of Bicyclo[4.2.1]non-1(4)-en-6-ones and Bicyclo[5.2.1]dec-1(10)-en-5-ones.
✍ Sharad K. Verma; Que H. Nguyen; James M. MacDougall; Everly B. Fleischer; Harold πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons βš– 36 KB πŸ‘ 1 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