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Sequential Ketene Generation from Dioxane-4,6-dione-keto-dioxinones for the Synthesis of Terpenoid Resorcylates
Trapping of the ketene generated from the thermolysis of 2-methyl-2-phenyl-1,3-dioxane-4,6-dione-keto-dioxinone at 50 °C with primary, secondary, or tertiary alcohols gave the corresponding dioxinone β-keto-esters in good yield under neutral conditions. These intermediates were converted by palladiu...
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Published in: | Organic letters 2016-04, Vol.18 (8), p.1800-1803 |
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container_end_page | 1803 |
container_issue | 8 |
container_start_page | 1800 |
container_title | Organic letters |
container_volume | 18 |
creator | Elliott, Daniel C Ma, Tsz-Kan Selmani, Aymane Cookson, Rosa Parsons, Philip J Barrett, Anthony G. M |
description | Trapping of the ketene generated from the thermolysis of 2-methyl-2-phenyl-1,3-dioxane-4,6-dione-keto-dioxinone at 50 °C with primary, secondary, or tertiary alcohols gave the corresponding dioxinone β-keto-esters in good yield under neutral conditions. These intermediates were converted by palladium(0)-catalyzed decarboxylative allyl migration and aromatization into the corresponding β-resorcylates. These transformations were applied to the syntheses of the natural products (±)-cannabiorcichromenic and (±)-daurichromenic acid. |
doi_str_mv | 10.1021/acs.orglett.6b00533 |
format | article |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Benzopyrans - chemical synthesis Benzopyrans - chemistry Biological Products - chemical synthesis Biological Products - chemistry Catalysis Chromans - chemical synthesis Chromans - chemistry Dioxanes - chemistry Ethylenes - chemistry Ketones - chemistry Molecular Structure Palladium - chemistry Stereoisomerism Terpenes - chemical synthesis Terpenes - chemistry |
title | Sequential Ketene Generation from Dioxane-4,6-dione-keto-dioxinones for the Synthesis of Terpenoid Resorcylates |
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