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The Stereochemistry of the Camphoketene Dimers 1

โœ Scribed by Baldwin, John E.


Book ID
118207576
Publisher
American Chemical Society
Year
1964
Tongue
English
Weight
237 KB
Volume
29
Category
Article
ISSN
0022-3263

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๐Ÿ“œ SIMILAR VOLUMES


The camphoketene dimers
โœ Peter Yates; E.A. Chandross ๐Ÿ“‚ Article ๐Ÿ“… 1959 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 234 KB

TREATMENT of an ethereal solution of d-camphor-3-carbonyl chloride (I) with quinoline or triethylamine yields two isomeric products, C&iS804, which . were considered by Staudlnger and SchotzL to be stereoisomers of the l,?Lcyclobutauedione derivative II, arising by dimerizatlon of "camphoketene" (II

The stereochemistry of allene dimerizati
โœ Thomas L. Jacobs; Oliver J. Muscio Jr. ๐Ÿ“‚ Article ๐Ÿ“… 1970 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 196 KB

In the previous papers in this series we have demonstrated that dimerization of acyclic allenes exhibits a stereoselectivity which favors the formation of those isomers in which the exocyclic methylene substituents take the inward, more crowded orientation. This stereoselectivity was attributed to f