Abstract
Enamines of cyclic ketones were α-alkylthiolated in good yields by simply refluxing them with alkyl 4-methylbenzenethiosulfonates and triethylamine in acetonitrile.
Literatur
10. Mitt.:Scholz D., Liebigs Ann. Chem., im Druck.
Review:Trost B. M., Chem. Rev.78, 363 (1978);Scholz D., Chem. Ber.114, 909 (1981);Scholz D., Liebigs Ann. Chem.1983, 98.
Scholz D., Liebigs Ann. Chem., im Druck.
Scholz D., Manuskript in Vorbereitung.
Woodward R. B., Pachter I. J., Scheinbaum M. L., J. Org. Chem.36, 1137 (1971).
Scholz D., Synthesis1983, 944.
Stork, G., Brizzolara A., Laudesman H., Szmuszovicz J., Terrell R., J. Amer. Chem. Soc.85, 207 (1963).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Scholz, D. Neue Synthesemethoden, 11. Mitt. α-Alkylthiolierung von cyclischen Ketonen via ihre Enamine. Monatsh Chem 115, 655–657 (1984). https://doi.org/10.1007/BF00799174
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00799174