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- W3159122095 abstract "A selective and efficient synthesis of diaryl 1,3,5-oxadiazines was established for the first time from simple and readily available amidines in wet DMSO. DMSO was employed as a dual carbon synthon and water offered the oxygen atom to construct the oxadiazine ring. The reaction involved two new C–N and two new C–O bond formations." @default.
- W3159122095 created "2021-05-10" @default.
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- W3159122095 date "2021-05-03" @default.
- W3159122095 modified "2023-10-16" @default.
- W3159122095 title "DMSO as a Dual Carbon Synthon and Water as Oxygen Donor for the Construction of 1,3,5-Oxadiazines from Amidines" @default.
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- W3159122095 doi "https://doi.org/10.1021/acs.orglett.1c01116" @default.
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