A novel method of annelation
โ Scribed by C. Schmidt; J. Thazhuthaveetil
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- French
- Weight
- 91 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
In our studies toward the total synthesis of deca-nor trlterpenoids 1.2
we were required to develop a method of annelatlon which allows the incorporation of an angular methyl group and a ketone group at position 11 In quassin 3
The potentiality of general application of this reaction Rrompts us to communicate our results at the present time as applied to 2,6-dimethyl-cyclohexanone
(1). The following sequence provides a 50% overall yield in three steps.
๐ SIMILAR VOLUMES
The cyclization of the A-ring involves the first case of an anionic elkvlation of an anthraquinone at a nosition which is not ortho to a phenolic function.