𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The stereochemistry of the cyclopropane-allene conversion

✍ Scribed by W.M. Jones; John W. Wilson Jr.


Book ID
108383223
Publisher
Elsevier Science
Year
1965
Tongue
French
Weight
203 KB
Volume
6
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


The Stereochemistry of Carbenoid Cyclopr
✍ Hans Christian Stiasny; Reinhard W. Hoffmann πŸ“‚ Article πŸ“… 1995 πŸ› John Wiley and Sons 🌐 English βš– 670 KB

The stereochemical course of the intramolecular carbenoid cyclopropanation reaction has been studied for the epimeric carbenoids 12a and 12b. In these reactions the terl-butyldimethylsilyloxy substituent serves as an internal stereochemical reference point. It was found that 12b cyclizes rapidly at

The stereochemistry of the palladium-cat
✍ L. Crombie; P.A. Jenkins; D.A. Mitchard; J.C. Williams πŸ“‚ Article πŸ“… 1967 πŸ› Elsevier Science 🌐 French βš– 322 KB

An allene of appropriate substitution has four distinguishable attitudes of presentation to a solid catalyst (Ip-IVp) leading by 1,2-a-addition to four different olefins (I-IV). (Received in UK 30 June 1967) on approach of the oriented allene to the catalyst might be expected to be important whether

The stereochemistry of the cleavage of c
✍ Frederick R. Jensen; Dennis B. Patterson; Stephen E. Dinizo πŸ“‚ Article πŸ“… 1974 πŸ› Elsevier Science 🌐 French βš– 236 KB

Because of the current interest2 in the stereochemistry of electrophilic aliphatic substitution, we with to report the results of reaction of 7,7-dimethylnorcarane, I, and norcarane with mercuric acetate. Cleavage of 1 in methanol (30 hrs, 25') after filtration to remove mercurous acetate (10%) and