The work presented herein describes the synthesis of a formerly inaccessible class of heterocyclic compounds. The reaction relies on α-phthalimido-amides, which are readily prepared from amino acids in 2 simple reactions steps. Under amide activation conditions in which classical keteniminium ions are not formed, the nitrile solvent is incorporated into the new fused 7-membered ring system. Due to the absence of a keteniminium intermediate, the stereogenic information in the α-position is fully retained.
Keywords: 7‐Membered rings; Amide activation; Cyclization; Heterocycles; Synthetic methods.
© 2020 The Authors. Published by Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim.