sameAs
EvOligo: A Novel Software to Design and Group Libraries of Oligonucleotides Applicable for Nucleic Acid-Based Experiments.Gel electrophoresis in a polyvinylalcohol coated fused silica capillary for purity assessment of modified and secondary-structured oligo- and polyribonucleotides.Application of click chemistry to the production of DNA microarrays.Novel method of synthesis of 5''-phosphate 2'-O-ribosyl-ribonucleosides and their 3'-phosphoramidites.Thermolytic carbonates for potential 5'-hydroxyl protection of deoxyribonucleosides.Conceptual "Heat-Driven" approach to the synthesis of DNA oligonucleotides on microarrays.2-Pyridinyl-N-(2,4-difluorobenzyl)aminoethyl Group As Thermocontrolled Implement for Protection of Carboxylic Acids.The "Clickable" Method for Oligonucleotide Immobilization Onto Azide-Functionalized Microarrays.Modulating the Stability of 2-Pyridinyl Thermolabile Hydroxyl Protecting Groups via the "Chemical Switch" Approach.Experimental and computational studies on a protonated 2-pyridinyl moiety and its switchable effect for the design of thermolytic devicesInvestigations on Synperiplanar and Antiperiplanar Isomers of Losartan: Theoretical and Experimental NMR Studies.The 2-(N-formyl-N-methyl)aminoethyl group as a potential phosphate/thiophosphate protecting group in solid-phase oligodeoxyribonucleotide synthesisProtecting of a thermolabile protecting group: "click-clack" approachOxidation of H-phosphonates with iodine by intramolecular support of a 2-pyridyl thermolabile protecting group2-Pyridinyl Thermolabile Groups as General Protectants for Hydroxyl, Phosphate, and Carboxyl FunctionsFluorescent 2-(Pyridin-2-yl)vinyl Pyridine Dyes and Their Thermocontrolled Release
P50
Q36308301-901BCFD9-70A2-47E0-8DE7-CF4B0D1AE462Q36499874-BB9279CF-7147-44AD-AAD0-F7F7501816ABQ38327874-5F6F7147-B9EC-43BD-B314-DA68FAF89BE2Q43604801-D26F6D63-AAA5-4A4F-8DCA-65FD33CA3096Q44698134-960E05E1-73F4-4962-BEE9-EC19671B9221Q44748705-10353CD2-EB40-4319-AA8B-0C7A92EE9E8DQ50793644-6E5E5B26-3DE5-4675-9280-DA176F01F748Q53183499-280C5BBE-7E20-41DE-A208-BF7C80604673Q53657716-5FC223B8-6413-4573-8B35-C96BBF17E36CQ58713378-99CD51EA-AC22-4587-AA7A-EFE5B0FE6383Q64924007-34F79910-B58F-47BB-83F1-ECA5EB0576CAQ73868289-7E66B52B-8148-4E47-A2AC-12107894D970Q84495410-79806CD2-92C0-4F66-B7DC-46A0FC855817Q84834239-05B60FF2-24EF-4792-BA34-0B9FE73582DCQ89393583-067CAC59-ED0A-4C2C-B841-709828BDD64EQ90452062-8AB3FA8C-DA24-497E-B2C7-A9BC2970DBC4
P50
description
polski chemik
@pl
researcher ORCID ID = 0000-0001-5717-7139
@en
wetenschapper
@nl
name
Marcin Chmielewski
@pl
Marcin K Chmielewski
@ast
Marcin K Chmielewski
@en
Marcin K Chmielewski
@es
Marcin K Chmielewski
@nl
type
label
Marcin Chmielewski
@pl
Marcin K Chmielewski
@ast
Marcin K Chmielewski
@en
Marcin K Chmielewski
@es
Marcin K Chmielewski
@nl
altLabel
Marcin K. Chmielewski
@pl
prefLabel
Marcin Chmielewski
@pl
Marcin K Chmielewski
@ast
Marcin K Chmielewski
@en
Marcin K Chmielewski
@es
Marcin K Chmielewski
@nl
P214
P106
P1153
56825349000
P214
P31
P496
0000-0001-5717-7139
P734
P735
P7859
viaf-315208471