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- W2010330735 abstract "The addition of lithium carbenoids to isocyanates provides a versatile access to N-substituted 2-haloacetamides: the reaction tolerates the presence of variously functionalized substituents on the nitrogen atom, including sterically demanding ones and reactive halogens. No erosion of the enantiopurity was observed in the case of optically active isocyanates. One of the substrates prepared has been employed in Charette's type chemoselective addition of a Grignard reagent to access an α-chloroketone." @default.
- W2010330735 created "2016-06-24" @default.
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- W2010330735 date "2013-01-01" @default.
- W2010330735 modified "2023-10-16" @default.
- W2010330735 title "Addition of lithium carbenoids to isocyanates: a direct access to synthetically useful N-substituted 2-haloacetamides" @default.
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- W2010330735 doi "https://doi.org/10.1039/c3cc44255a" @default.
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