The present invention relates to a use of a cyclic imidate as a ligand for catalysis in which the ligand contains sub-structure (Y) as a minimal structural motive, wherein the carbon atoms and the nitrogen atom can be optionally substituted by a chemical substituent.
This disclosure relates to compounds of formula (I), which are modulators of STING. Also disclosed are pharmaceutical compositions comprising compounds of formula (I) and methods of using compounds of formula (I) in the treatment or prevention of diseases ameliorated by the modulation of STING.
[EN] SUBSTITUTED AMIDOBENZIMIDAZOLE DIMERS AS STING MODULATORS<br/>[FR] DIMÈRES D'AMIDOBENZIMIDAZOLE SUBSTITUÉS EN TANT QUE MODULATEURS DE STING
申请人:ACULEUS THERAPEUTICS PTY LTD
公开号:WO2022266711A1
公开(公告)日:2022-12-29
This disclosure relates to compounds of formula (I), which are modulators of STING. Also disclosed are pharmaceutical compositions comprising compounds of formula (I) and methods of using compounds of formula (I) in the treatment or prevention of diseases ameliorated by the modulation of STING.
Efficient one-step synthesis of chiral bidentate oxazoline-alcohol ligands via a cyclic imidate ester rearrangement
作者:Timothy Noël、Koen Robeyns、Luc Van Meervelt、Erik Van der Eycken、Johan Van der Eycken
DOI:10.1016/j.tetasy.2009.07.038
日期:2009.9
Various chiral bidentate oxazoline-alcohol ligands were obtained in a straightforward one-step synthesis via a cyclic imidate ester rearrangement. These chiral ligands were tested and compared in asymmetric diethylzinc additions to aldehydes resulting in selectivities of up to 87% ee. An interesting chirality switch was observed when a CPh2-tether instead of a CH2 was present, offering the opportunity for dual stereocontrol. (C) 2009 Elsevier Ltd. All rights reserved.