Inhibitors of cholesterol biosynthesis. 3. Tetrahydro-4-hydroxy-6-[2-(1H-pyrrol-1-yl)ethyl]-2H-pyran-2-one inhibitors of HMG-CoA reductase. 2. Effects of introducing substituents at positions three and four of the pyrrole nucleus
about
An overview of the key routes to the best selling 5-membered ring heterocyclic pharmaceuticals.Structure-based design of potent Bcl-2/Bcl-xL inhibitors with strong in vivo antitumor activity.A potent and highly efficacious Bcl-2/Bcl-xL inhibitor.Carbene catalystsMethyl 1-benzyl-5-methyl-2,4-diphenyl-1H-pyrrole-3-carboxyl-ate.A continuum of progress: applications of N-hetereocyclic carbene catalysis in total synthesis.Diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams.HMG-CoA Reductase inhibitors: an updated review of patents of novel compounds and formulations (2011-2015).Conformational analysis of geometric isomers of pitavastatin together with their lactonized analogues.Rapid proteasomal elimination of 3-hydroxy-3-methylglutaryl-CoA reductase by interferon-γ in primary macrophages requires endogenous 25-hydroxycholesterol synthesis.rac-2-[2-(4-Fluoro-phen-yl)-2-oxo-1-phenyl-eth-yl]-4-methyl-3-oxo-N-phenyl-penta-namideAn improved kilogram-scale preparation of atorvastatin calcium.Functional-group-tolerant, nickel-catalyzed cross-coupling reaction for enantioselective construction of tertiary methyl-bearing stereocenters.Streamlined catalytic asymmetric synthesis of atorvastatin.Lipid-lowering effects of ethyl 2-phenacyl-3-aryl-1H-pyrrole- 4-carboxylates in rodents.Visible-light-induced formal [3+2] cycloaddition for pyrrole synthesis under metal-free conditions.Synthesis of Dihydropyrrolizine and Tetrahydroindolizine Scaffolds from Pyrroles by Titanocene(III) Catalysis.Synthesis of Pyrroles by Click Reaction: Silver-Catalyzed Cycloaddition of Terminal Alkynes with IsocyanidesApplications of organocatalysed visible-light photoredox reactions for medicinal chemistry
P2860
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P2860
Inhibitors of cholesterol biosynthesis. 3. Tetrahydro-4-hydroxy-6-[2-(1H-pyrrol-1-yl)ethyl]-2H-pyran-2-one inhibitors of HMG-CoA reductase. 2. Effects of introducing substituents at positions three and four of the pyrrole nucleus
description
1991 nî lūn-bûn
@nan
1991 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Inhibitors of cholesterol bios ...... nd four of the pyrrole nucleus
@ast
Inhibitors of cholesterol bios ...... nd four of the pyrrole nucleus
@en
Inhibitors of cholesterol bios ...... nd four of the pyrrole nucleus
@nl
type
label
Inhibitors of cholesterol bios ...... nd four of the pyrrole nucleus
@ast
Inhibitors of cholesterol bios ...... nd four of the pyrrole nucleus
@en
Inhibitors of cholesterol bios ...... nd four of the pyrrole nucleus
@nl
prefLabel
Inhibitors of cholesterol bios ...... nd four of the pyrrole nucleus
@ast
Inhibitors of cholesterol bios ...... nd four of the pyrrole nucleus
@en
Inhibitors of cholesterol bios ...... nd four of the pyrrole nucleus
@nl
P2093
P356
P1476
Inhibitors of cholesterol bios ...... nd four of the pyrrole nucleus
@en
P2093
A W Chucholowski
C D Stratton
C J Blankley
C S Sekerke
D F Ortwine
D R Sliskovic
E Ferguson
M L Hoefle
R S Newton
P304
P356
10.1021/JM00105A056
P407
P577
1991-01-01T00:00:00Z