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Journal ArticleDOI

Syntheses in the cyclohexanone series. II. The syntheses of 4-Ethylcyclohex-2- enone, 4-Ethylcyclohex-3-enone, and 4-Ethylidenecyclohexanone

KG Lewis, +1 more
- 01 Jan 1970 - 
- Vol. 23, Iss: 4, pp 807-812
TLDR
In this article, a Robinson-type ring closure was used to synthesize 4-ethylcyclohex-2-enone by a mixture of conjugated and non-conjugated ketones.
Abstract
An attempt to synthesize 4-ethylcyclohex-2-enone by a Robinson-type ring closure gave a mixture of conjugated and non-conjugated ketones from which the conjugated isomer was isolated. 4-Ethylcyclohex-3-enone on treatment with acid yielded the same mixture of ketones. Pyrolysis of 4-carboxy-4-vinylheptanedioic acid with barium carbonate formed 4-ethylidenecyclohexanone.

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Journal ArticleDOI

Recent developments in the chemistry of sandalwood odorants

TL;DR: The preparation of the novel sandalwood odorants 26, 33, and 39 will be discussed, including their sensory properties and structure–odor relationship.
Journal ArticleDOI

Intermediates for the synthesis of indole alkaloids. Synthesis of tetrahydrocarbazole derivatives

TL;DR: In this paper, the synthesis of new precursors 8 and 15 for the tetracyclic indole alkaloids was described, and many new intermediates 4-7 and 9-14 have also been synthesized.
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