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- W3135367036 endingPage "1757" @default.
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- W3135367036 abstract "Abstract A useful aminohalogenation reaction for the cyclization of O ‐alkynyl carbamates under copper catalysis has been developed. N ‐Halosuccinimides have been used as a halogen source. The intramolecular C−N bond formation occurs selectively affording haloalkylidene substituted heterocycles. Just in the case of α,α‐cyclohexyl‐substituted propargyl carbamate, the alkoxyhalogenation pathway was operative. The mechanism for the two alternative reaction pathways was investigated by modeling the corresponding transition states at the DFT level." @default.
- W3135367036 created "2021-03-15" @default.
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- W3135367036 date "2021-03-15" @default.
- W3135367036 modified "2023-10-18" @default.
- W3135367036 title "Copper(II)‐Catalyzed Aminohalogenation of Alkynyl Carbamates" @default.
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- W3135367036 doi "https://doi.org/10.1002/ejoc.202100202" @default.
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