Synthesis of Chromeno[3,4-<i>b</i>]piperazines by an Enol-Ugi/Reduction/Cyclization Sequence
Keto piperazines and aminocoumarins are privileged building blocks for the construction of geometrically constrained peptides and therefore valuable structures in drug discovery. Combining these two heterocycles provides unique rigid polycyclic peptidomimetics with drug-like properties including man...
Main Authors: | Ana Bornadiego, Ana G. Neo, Carlos F. Marcos |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-02-01
|
Series: | Molecules |
Subjects: | |
Online Access: | https://www.mdpi.com/1420-3049/26/5/1287 |
Similar Items
-
Amide-Stabilized Enols in the Enol-Ugi Reaction: A Five-Component Synthesis of Triamides
by: Ana G. Neo, et al.
Published: (2021-11-01) -
Diastereoselective Ugi reaction of chiral 1,3-aminoalcohols derived from an organocatalytic Mannich reaction
by: Samantha Caputo, et al.
Published: (2016-01-01) -
Isocyanide-based multicomponent reactions towards cyclic constrained peptidomimetics
by: Gijs Koopmanschap, et al.
Published: (2014-03-01) -
Multicomponent synthesis of artificial nucleases and their RNase and DNase activity
by: Anton V. Gulevich, et al.
Published: (2011-08-01) -
Studies on the interaction of isocyanides with imines: reaction scope and mechanistic variations
by: Ouldouz Ghashghaei, et al.
Published: (2014-01-01)