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Conjugate addition of lithium diorganocuprate reagents to the enol tosylate of a 1,2-diketone

โœ Scribed by Jeffrey A. Charonnat; Anna L. Mitchell; Bartholomew P. Keogh


Publisher
Elsevier Science
Year
1990
Tongue
French
Weight
207 KB
Volume
31
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


The conjugate addition of lithium diorganocupmte reagents to the enol tosylate of 1,2cyclohexanedione has been investigated. The intermediate enolates eliminatepara-toluenesulfiiate ion to generate the alkylated 1,2-dicarbonyl system.


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Regioselectivity in the conjugate additi
โœ James A. Marshall; Ronald A. Ruden; Larry K. Hirsch; Mark Phillippe ๐Ÿ“‚ Article ๐Ÿ“… 1971 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 183 KB

The conjugate addition of organometallic reagents to en&es constitutes a useful, and often highly selective alkylation method. A number of studies have been carried out on conjugated