propargyl isocyanides were reacted under the conditions of Passerini and Ugi reactions. They led to α-acyloxy amides and α-amino amides with an unsaturated substituent on the nitrogen atom in reasonable yields. Some of them were then functionalized thanks to the pending unsaturation, opening the field of complex products in subsequent reactions.
动力学不稳定的乙烯基、丙二烯基和炔丙基异氰化物在 Passerini 和 Ugi 反应条件下反应。他们以合理的产率产生了在氮原子上具有不饱和取代基的 α-酰氧基酰胺和 α-氨基酰胺。由于待定的不饱和度,其中一些随后被官能化,为后续反应中的复杂产品领域开辟了道路。