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- W1966471570 abstract "The allylic alcohols 1 obtained from lithiated 1,4-dioxene and ketones or aldehydes undergo regiospecifically oxidative cleavage with pyridinium chlorochromate at the dioxene double bond to give, after saponification, α-hydroxy acids. Extension of this reaction to α,β-unsaturated ketones 10 affords α-keto acids." @default.
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- W1966471570 date "1988-01-01" @default.
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- W1966471570 title "1,4-dioxene in organic chemistry. Part VII regiospecific oxidative cleavage of 1,4-dioxenyl carbinols with pyridinium chlorochromate. A new method for the preparation of α-hydroxy acids and α-keto acids." @default.
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- W1966471570 doi "https://doi.org/10.1016/s0040-4039(00)82320-5" @default.
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