Methodology for the conversion of tetramates to pyroglutamates, and a study of their biological activity
<p>Highly functionalised pyroglutamates, molecules of interest for their biological uses and applications, are readily accessible from a bicyclic tetramic acid as a substrate for functionalisation at C3 and C4 of tetramic acid ring. These molecules have structural features common to pyroglutam...
Main Author: | Bagum, H |
---|---|
Other Authors: | Moloney, M |
Format: | Thesis |
Published: |
2018
|
Similar Items
-
Synthetic access to 3,4-disubstituted pyroglutamates from tetramate derivatives from serine, allo-threonine and cysteine
by: Bagum, H, et al.
Published: (2019) -
Synthetic access to 3-substituted pyroglutamic acids from tetramate derivatives of serine, threonine, allo-threonine, and cysteine
by: Bagum, H, et al.
Published: (2019) -
Diastereoselective reduction of the tricarbonyl moiety in bicyclic tetramates giving pyroglutamates
by: Josa-Culleré, L, et al.
Published: (2018) -
Highly functionalised pyroglutamates by intramolecular aldol reactions: Towards the pyroglutamate skeleton of oxazolomycin
by: Andrews, MD, et al.
Published: (1996) -
Metabolic Acidosis Due To Pyroglutamic Acid
by: Maria João Raposo Linhares Serpa, et al.
Published: (2018-09-01)