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The stereochemistry of the Michael addition reaction. The synthesis of trans-3,5 - dimethylcyclohexanone

โœ Scribed by Norman L. Allinger; C.K. Riew


Publisher
Elsevier Science
Year
1966
Tongue
French
Weight
192 KB
Volume
7
Category
Article
ISSN
0040-4039

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๐Ÿ“œ SIMILAR VOLUMES


Stereochemistry of the Michael addition.
โœ R.A. Abramovitch; D.L. Struble ๐Ÿ“‚ Article ๐Ÿ“… 1966 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 234 KB

The Michael Addition has usually been studied under conditions such and J. M. Muchowski. Can. J Chem 3f& 557 (1960). U A\* No.3 2. Correct analyzes were obtained for all the new compounds mentioned here. Reaction mixtures were analyzed quantitatively and qualitatively by gas-liquid chromatography.

The Michael reaction of acetophenones wi
โœ Mohammad M Al-Arab; Mohammad A Atfeh; Fowzia S Al-Saleh ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 477 KB

The synthesis of a series of highly substituted cyclohexane derivatives has been carried out in a single one-pot reaction of acetophenones and lrnfl.s-dibenzoylethylene (12) using sodium ethoxide in anhydrous diethyl ether at room temperature to give 4-aroyl-2,3,5tribenzoyl-I-phenylcyclohexanols A s