| Structure Identification: |
| Bulletin of the Chemical Society of Japan, 1990, 63(9):2540-2548. | | Syntheses and Reactions of Conjugated Dienic Thioketones.[Reference: WebLink] |
METHODS AND RESULTS:
5,6-Dihydro-2-phenyl-3-thiobenzoyl-2H-naphtho[1,2-b]thiin (8a) and the related dienic thioketones were synthesized in 3 steps starting from 2-(phenylthio)methylenetetralin-1-thione with chalcone, 4′-chrolochalcone, 4'-Methoxychalcone, 2-cinnamoylthiophen, 2-cinnamoylfuran, 1-phenyl-2-buten-1-one, and acrylophenone respetively. Similarly, 3-thiobenzoyl-2,6-diphenyl-2H-thiin (8i) was synthesized from 1-phenyl-3-phenylthio-2-propene-1-thione. All of these dienic thioketones were found to exist in stable monomeric form. The conjugated dienic thioketone (8a) reacted as α,β-unsaturated thioketone with 2-norbornene, 2,5-norbornadiene, diethyl azodicarboxylate, diphenyl fumarate, N-phenyl- and N-(p-tolyl)maleimides, 2-chloroacrylonitrile, methyl methacrylate, acrylonitrile, and styrene to give the corresponding [4+2]cycloadducts. The thioketone (8i) also reacted with 2-norbornene to give the corresponding cycloadduct.
CONCLUSIONS:
The reaction provides a useful method for the syntheses of various sulfur-containing heterocycles. |
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