Synthesis of endo-1,3-dimethyl-2,9-dioxa
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Peter Mohr; Christoph Tamm
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Article
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1987
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Elsevier Science
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French
β 112 KB
The title compound has been synthesized stereoselectively based on a new methodology for the construction of erythro-1,3-diols. Endo-1,3-dimethyl-2,9-dioxabicyclo[3.3.1]nonane (11, first isolated by Heemann and Francke in 1976 from Norway spruce attacked by the ambrosia beetle (Tgypodendron Lineatum