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- W2758095744 abstract "Abstract A Regioselective and efficient synthesis of α,α‐diiodo‐α′‐acetoxyketones as well as α,α‐dibromo‐α′ ‐acetoxyketones has been achieved from the propargylic acetates and N ‐iodo(bromo)succinimides in the absence of any added promoters. This transformation is very general and shown compatibility for all structural types of propargylic acetates with terminal alkyne unit, such as tertiary ‐ (aryl‐aryl; aryl‐alkyl; alkyl‐alkyl), secondary‐ (aryl; alkyl), primary‐; and hence provided access to structurally divergent and highly important halogenated building blocks." @default.
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- W2758095744 date "2017-09-21" @default.
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- W2758095744 title "An Expeditious Approach to α,α-Dihalo-α′-acetoxyketones from Propargylic Acetates" @default.
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- W2758095744 doi "https://doi.org/10.1002/slct.201701398" @default.
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