Hydantoin bioisosteres. In vivo active spiro hydroxy acetic acid aldose reductase inhibitors.
about
Asymmetric Methods for the Synthesis of Flavanones, Chromanones, and AzaflavanonesSynthesis of substituted chromanones: an organocatalytic aldol/oxa-Michael reaction.Bioactivity Focus of α-Cyano-4-hydroxycinnamic acid (CHCA) Leads to Effective Multifunctional Aldose Reductase Inhibitors.Pharmacophore modeling, molecular docking, and molecular dynamics simulation approaches for identifying new lead compounds for inhibiting aldose reductase 2.Minimizing Aryloxy Elimination in Rh(I) -Catalyzed Asymmetric Hydrogenation of β-Aryloxyacrylic Acids using a Mixed-Ligand Strategy.Annulation of Alkynyl Aryl Ethers with Allyl Pivalates To Give 2,3-Bismethylenechromanes through Double C-H Bond Cleavage.
P2860
Hydantoin bioisosteres. In vivo active spiro hydroxy acetic acid aldose reductase inhibitors.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Hydantoin bioisosteres. In viv ...... d aldose reductase inhibitors.
@en
type
label
Hydantoin bioisosteres. In viv ...... d aldose reductase inhibitors.
@en
prefLabel
Hydantoin bioisosteres. In viv ...... d aldose reductase inhibitors.
@en
P2093
P356
P1476
Hydantoin bioisosteres. In viv ...... d aldose reductase inhibitors.
@en
P2093
C E Aldinger
D L Bussolotti
P B Inskeep
T W Siegel
P304
P356
10.1021/JM00090A004
P407
P577
1992-06-01T00:00:00Z