๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

The intramolecular Michael addition as a route to angularly substituted cis-hydrindanes

โœ Scribed by Gilbert Stork; Douglass F. Taber; Michael Marx


Publisher
Elsevier Science
Year
1978
Tongue
French
Weight
194 KB
Volume
19
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

โœฆ Synopsis


Cis-hydrindane derivatives carrying an angular substituent and suitably functionalized are of interest, inter alia, for the construction of natural products such as the gibberellic acids.


๐Ÿ“œ SIMILAR VOLUMES


Michael addition of ethyl acetoacetate t
โœ Andrey M Chibiryaev; Norbert De Kimpe; Alexey V Tkachev ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 69 KB

The FeCl 3 -catalyzed reaction of a,b-unsaturated oximes with ethyl acetoacetate resulted in Michael addition followed by ring closure to produce substituted nicotinic acid derivatives in a very efficient way.