Ruthenium catalyzed reactions of ethylene glycol with primary amines: steric factors and selectivity control
摘要:
The selectivity of reactions of ethylene glycol with primary amines in the presence of RuCl2(PPh3)3 at 120-degrees-C is highly dependent on the steric nature of the amine. Selectivity to di-amination is favored by smaller alkyl groups on the amine while large amines cleanly yield ethanolamines. This contrasts with the results obtained with secondary amines at this temperature, in which ruthenium-triphenylphosphine catalyst systems always favor mono-amination. In the case of sec-butyl amine, where almost equal amounts of mono- and di-aminated product are obtained, the selectivity can be shifted to mono-amination by the addition of excess triphenylphosphine. The steric effects seen in these reactions are consistent with standard steric parameters available from the literature.
[EN] SELECTIN OR GALECTIN ANTAGONISTS FOR TREATING CYTOKINE RELEASE SYNDROME AND CRS-INDUCED NEUROTOXICITY<br/>[FR] ANTAGONISTES DE LA SÉLECTINE OU DE LA GALECTINE POUR LE TRAITEMENT DU SYNDROME DE LIBÉRATION DE LA CYTOKINE ET DE LA NEUROTOXICITÉ INDUITE PAR LE CRS
申请人:MAGNANI JOHN L
公开号:WO2020150263A1
公开(公告)日:2020-07-23
Methods and compounds for the treatment and/or prevention of CRS and/or CRS-induced neurotoxicities using at least one selectin antagonist are disclosed. The disclosed methods and compounds use at least one of the disclosed antagonists to target and reduce cytokine expression and/or endothelial activation to treat and/or prevent CRS and/or CRS-related conditions such as CRS-induced neurotoxicities.
yields, and have therefore been neglected as fluorescentdyes. Here we investigate the fluorescence properties of diaminodicyanoquinones using a combined theoretical and experimental approach and derive molecules with a fluorescence quantum yield exceeding 90 %. The diaminodicyanoquinone core moiety provides chemical versatility and can be integrated into novel molecular architectures with unique photophysical
HETEROBIFUNCTIONAL INHIBITORS OF E-SELECTIN AND GALECTIN-3
申请人:GLYCOMIMETICS, INC.
公开号:US20200399301A1
公开(公告)日:2020-12-24
Compounds, compositions, and methods for treatment and/or prevention of at least one disease, disorder, and/or condition by inhibiting binding of an E-selectin, galectin-3, or E-selectin and galectin-3 to ligands a disclosed. For example, heterobifunctional inhibitors of E-selectin and galectin-3 are described and pharmaceutical compositions comprising at least one such agent is described.
GALACTOPYRANOSYL-CYCLOHEXYL DERIVATIVES AS E-SELECTIN ANTAGONISTS
申请人:GLYCOMIMETICS, INC.
公开号:US20220175808A1
公开(公告)日:2022-06-09
Compounds, compositions, and methods for treatment and/or prevention of at least one disease, disorder, and/or condition by inhibiting binding of an E-selectin to an E-selectin ligand are disclosed. For example, E-selectin antagonists are described and pharmaceutical compositions comprising at least one of the same.
Ruthenium catalyzed reactions of ethylene glycol with primary amines: steric factors and selectivity control
作者:John A. Marsella
DOI:10.1016/0022-328x(91)83143-r
日期:1991.4
The selectivity of reactions of ethylene glycol with primary amines in the presence of RuCl2(PPh3)3 at 120-degrees-C is highly dependent on the steric nature of the amine. Selectivity to di-amination is favored by smaller alkyl groups on the amine while large amines cleanly yield ethanolamines. This contrasts with the results obtained with secondary amines at this temperature, in which ruthenium-triphenylphosphine catalyst systems always favor mono-amination. In the case of sec-butyl amine, where almost equal amounts of mono- and di-aminated product are obtained, the selectivity can be shifted to mono-amination by the addition of excess triphenylphosphine. The steric effects seen in these reactions are consistent with standard steric parameters available from the literature.