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- W561786989 abstract "exo-3-Formy1-3-methylcamphor was synthesized by a following route, for the purpose of asymmetric alkylation of glycine.Methyl 3-methyl-3-camphorca rboxylates [4] were obtained by the methylation of methyl 3-camphorcarboxylate [3] with sodium hydride and methyl iodide in good yield. The products were separated into two parts by treating with ligroine, i. e. a crystalline part [4a](mp 88-48.5°C) and an oily one [4b]. It was found that the structure of [4a] was determined as exo-3-carboxylate and that of [4b] was as endo-one by the analyses of their NMR data. The reduction of [4a] with LiAlH4 gave diol[5] And exo-3-formy1-3-methylcampho r was obtained as a slightly unstable liquid (bp 123°C/13 mmHg, [α]D20 162.5°) by the oxida-tion of [5] with Collins' reagent." @default.
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- W561786989 date "1987-01-01" @default.
- W561786989 modified "2023-10-14" @default.
- W561786989 title "A synthesis of exo-3-formyl-3-methylcamphor." @default.
- W561786989 doi "https://doi.org/10.1246/nikkashi.1987.257" @default.
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