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Ketene thioacetal monoxides: Some conjugate addition-alkylation reactions leading to unsymmetrical 1,4-dicarbonyl systems

✍ Scribed by J.L. Herrmann; G.R. Kieczykowski; R.F. Romanet; R.H. Schlessinger


Book ID
104238649
Publisher
Elsevier Science
Year
1973
Tongue
French
Weight
195 KB
Volume
14
Category
Article
ISSN
0040-4039

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✦ Synopsis


In the foregoing communications, we have outlined both the preparation' and conjugate addition behavior' of an interesting class of two-carbon Michael receptors, ketene thioacetal monoxides. Receptors like I were found to undergo the Michael reaction with ester enolates of dis-