Heteroannulations of cyanoacetamide-based MCR scaffolds utilizing formamide

Heteroannulations of cyanoacetamide-based MCR scaffolds utilizing formamide

C1 chemistry has a central role in the efficient utilization of single-carbon molecules, contributing significantly to sustainability, innovation and economic growth across various sectors. In this study, we present an efficient and rapid method for synthesizing a variety of heteroannulated pyrimido...

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Bibliographic Details
Main Authors: Marios Zingiridis, Danae Papachristodoulou, Despoina Menegaki, Konstantinos G. Froudas, Constantinos G. Neochoritis
Format: Article
Language:English
Published: Beilstein-Institut 2025-01-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
2-amino-substituted heterocycles
cyanoacetamide
gewald reaction
multicomponent reaction (mcr)
pyrimidine
Online Access:https://doi.org/10.3762/bjoc.21.13
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https://doi.org/10.3762/bjoc.21.13

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