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- W2003183526 abstract "Easy to assemble! An enantioselective cascade Mannich intramolecular ring cyclization–tautomerization reaction of malononitrile with 2-hydroxyl N-protected α-amido sulfone is described (see scheme), which provides a new route to the synthesis of the privileged scaffold 2-amino-4H-chromene in high yields (up to 94 %) and with good to high enantiomeric excesses (74–89 % ee)." @default.
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- W2003183526 date "2011-05-25" @default.
- W2003183526 modified "2023-10-10" @default.
- W2003183526 title "Expeditious Assembly of a 2‐Amino‐4<i>H</i>‐chromene Skeleton by Using an Enantioselective Mannich Intramolecular Ring Cyclization–Tautomerization Cascade Sequence" @default.
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- W2003183526 doi "https://doi.org/10.1002/chem.201100927" @default.
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