Macrocyclic drugs and synthetic methodologies toward macrocycles
about
Recent advances in the understanding of antibiotic resistance in Clostridium difficile infectionSynthesis of Hybrid Cyclopeptides through Enzymatic MacrocyclizationEnzymatic Macrocyclization of 1,2,3-Triazole Peptide MimeticsQ28828613Conventional and alternative treatment approaches for Clostridium difficile infectionRing-Expansion Approach to Medium-Sized Lactams and Analysis of Their Medicinal Lead-Like Properties.Progress in the discovery of treatments for C. difficile infection: A clinical and medicinal chemistry review.How proteins bind macrocycles.Twisted amide electrophiles enable cyclic peptide sequencing.Harnessing C-H Activation of Benzhydroxamates as a Macrocyclization Strategy: Synthesis of Structurally Diverse Macrocyclic Isoquinolones.Synthesis and antibacterial evaluation of macrocyclic diarylheptanoid derivativesSynthesis and biological evaluation of palmyrolide A macrocycles as sodium channel blockers towards neuroprotection.Advances in the synthesis of glycosidic macrolides: clavosolides A-D and cyanolide A.Modular, One-Pot, Sequential Aziridine Ring Opening-S(N)Ar Strategy to 7-, 10-, and 11-Membered Benzo-Fused Sultams.Process Chemistry in Antiviral Research.Pyrazolo[1,5-a]pyrimidine-based macrocycles as novel HIV-1 inhibitors: a patent evaluation of WO2015123182.Modularity of RiPP Enzymes Enables Designed Synthesis of Decorated Peptides.Preparation of macrocyclic Z-enoates and (E,Z)- or (Z,E)-dienoates through catalytic stereoselective ring-closing metathesisStereoselective synthesis of macrocyclic peptides via a dual olefin metathesis and ethenolysis approach.Exo-selective reductive macrocyclization of ynals.Formation of amides: one-pot condensation of carboxylic acids and amines mediated by TiCl4.Synthesis of a 1,3-Bridged Macrobicyclic Enyne via Chemoselective Cycloisomerization Using Palladium-Catalyzed Alkyne-Alkyne Coupling.Bypassing the proline/thiazoline requirement of the macrocyclase PatG.A novel medium size lactam ring analoges as antibacterial agents: Synthesis, biological evaluation and molecular docking studies.Pseudomonas fluorescens Strain R124 Encodes Three Different MIO Enzymes.Macrolide Synthesis through Intramolecular Oxidative Cross-Coupling of Alkenes.Two-Step Synthesis of Complex Artificial Macrocyclic Compounds.Characterization of the Fast and Promiscuous Macrocyclase from Plant PCY1 Enables the Use of Simple Substrates.Synthesis, structure and reactivity of [15]-macrodilactones.Predicting bioactive conformations and binding modes of macrocycles.Clostridium difficile Infections: A Global Overview of Drug Sensitivity and Resistance Mechanisms.A Brief Overview of Two Major Strategies in Diversity-Oriented Synthesis: Build/Couple/Pair and Ring-DistortionNucleoside macrocycles formed by intramolecular click reaction: efficient cyclization of pyrimidine nucleosides decorated with 5'-azido residues and 5-octadiynyl side chains
P2860
Q26767079-C462421B-9CE3-40DB-9F64-0CBE7207676EQ28817636-9F31222D-AB0F-462D-AA48-72581DC7F2A0Q28828607-3DD671D6-FAD8-4BDE-A144-45BEBA036B4BQ28828613-B9B13C81-F7FA-451A-8C6B-C7AFBE0554D1Q30235278-F461A1A4-9A94-4A2A-B577-AC61B449A88DQ30490492-216CDB66-511B-4009-9E74-D0FE048329B2Q35044119-F8D1F8A6-B9D6-43C1-B9D2-BC415A12287DQ35209183-3E1C24EB-6F3D-48EB-BCA9-6966879831D1Q35664642-9D960857-E846-4F69-A6F4-181A4C4408A8Q36028073-C49F1AB3-F823-42C5-9486-135AAFE72663Q36074415-7427FA48-3994-486A-8348-1B1CAAE43B36Q36106585-00264601-9CB8-4111-B465-F4E2EA09304EQ36156057-98A43B67-3198-498E-AA6A-1DE8A2FC9DA2Q37091004-4EC75CB9-8919-4900-BD9A-23F35A0ECC53Q38997200-F6A41552-107D-4178-9744-42D50E4B359DQ40618808-660862F0-7044-4C40-AE5D-77A27D289B85Q40747661-EC4E6B57-42CD-499E-8B87-AD7E6091162DQ42011298-9CC96D7A-C3FF-4CD3-B62C-27D8838AA32EQ42597666-D8E2F8B8-4EC6-4707-8A62-6F78C3E6BBEBQ42654406-CA7D10D8-8AF6-4C08-A04D-8E6EE1412392Q42737134-76D0DE8A-54E2-42B9-9528-6B5B3E25ED8BQ46950027-BF793D57-6F48-43B6-9B79-12E910F1C618Q47137366-434341F5-ADA3-4C9A-B4F1-EADF5F126FADQ47159106-929B55DF-E18C-47A4-A472-1E2DB588C53AQ47174569-ECB1339F-E6E9-40C6-8E43-750DC5BC496FQ47591730-1CACDD90-CA07-4D93-A60C-2C7BAEE2BADFQ48152859-97B6E11A-DB15-4E05-953B-8F80FFFF87C2Q49607196-D545834A-88F2-4939-8594-9D359A45E84DQ50974615-CAA49600-9B13-4813-8B88-97E4229CF2F1Q51477064-8206DA5E-6460-4541-87A1-7F940600FBFBQ53692769-422FA5AA-E57E-4B28-B7FA-1806E9533BECQ58580325-EFB75A67-9A28-4A24-8346-E9585A2B43FFQ58743375-3B607D85-17D9-4189-A0CB-67DF99C0F35E
P2860
Macrocyclic drugs and synthetic methodologies toward macrocycles
description
2013 nî lūn-bûn
@nan
2013 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
name
Macrocyclic drugs and synthetic methodologies toward macrocycles
@ast
Macrocyclic drugs and synthetic methodologies toward macrocycles
@en
Macrocyclic drugs and synthetic methodologies toward macrocycles
@nl
type
label
Macrocyclic drugs and synthetic methodologies toward macrocycles
@ast
Macrocyclic drugs and synthetic methodologies toward macrocycles
@en
Macrocyclic drugs and synthetic methodologies toward macrocycles
@nl
prefLabel
Macrocyclic drugs and synthetic methodologies toward macrocycles
@ast
Macrocyclic drugs and synthetic methodologies toward macrocycles
@en
Macrocyclic drugs and synthetic methodologies toward macrocycles
@nl
P2860
P921
P1433
P1476
Macrocyclic drugs and synthetic methodologies toward macrocycles
@en
P2093
Dianqing Sun
P2860
P304
P356
10.3390/MOLECULES18066230
P407
P577
2013-05-24T00:00:00Z