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- W2105316755 endingPage "8646" @default.
- W2105316755 startingPage "8643" @default.
- W2105316755 abstract "An efficient and practical one-pot approach to aza-Morita−Baylis−Hillman adducts has been developed. The reaction occurs between N-Boc or N-Cbz imines, generated in situ from stable and easy to handle N-Boc or N-Cbz protected α-amidoalkyl-p-tolylsulfones, and electron-deficient alkenes in the presence of DABCO. The presented procedure eliminates the use of the relatively unstable N-carbamate imines prior to the coupling reaction. The reaction is limited to α-amidosulfones derived from aromatic and heteroaromatic aldehydes." @default.
- W2105316755 created "2016-06-24" @default.
- W2105316755 creator A5019489501 @default.
- W2105316755 creator A5032901219 @default.
- W2105316755 date "2008-09-27" @default.
- W2105316755 modified "2023-10-10" @default.
- W2105316755 title "<i>N</i>-Carbamate Protected α-Amidoalkyl-<i>p</i>-tolylsulfones: Convenient Substrates in the aza-Morita−Baylis−Hillman Reaction" @default.
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