about
Structure analysis and conformational transitions of the cell penetrating peptide transportan 10 in the membrane-bound state.An entry into hexahydro-2H-thieno[2,3-c]pyrrole 1,1-dioxide derivatives.Focused enumeration and assessing the structural diversity of scaffold libraries: conformationally restricted bicyclic secondary diamines.Controlling biological activity with light: diarylethene-containing cyclic peptidomimetics.What Goes around Comes around-A Comparative Study of the Influence of Chemical Modifications on the Antimicrobial Properties of Small Cyclic Peptides.Cyclobutane-derived diamines: synthesis and molecular structure.Compatibility of the conformationally rigid CF3-Bpg side chain with the hydrophobic coiled-coil interface.Synthesis of 2-azaspiro[3.3]heptane-derived amino acids: ornitine and GABA analogues.Structure and chemistry of a zwitterionic amine-aldehyde adduct.3,5,7-trimethyl-1-azatricyclo[3.3.1.1(3,7)]decan-2-ylidene, an aminocarbene without pi conjugation.Synthesis of a new chiral bisphospholane ligand for the Rh(I)-catalyzed enantioselective hydrogenation of isomeric beta-acylamido acrylates.Highly stereoselective, thermodynamically controlled and reversible formation of a new P-chiral phosphine.4-Fluoro-2,4-methanoproline.Synthesis of trifluoromethyl-substituted proline analogues as 19F NMR labels for peptides in the polyproline II conformation.Direct Photocontrol of Peptidomimetics: An Alternative to Oxygen-Dependent Photodynamic Cancer Therapy.Solid state 19F NMR parameters of fluorine-labeled amino acids. Part II: aliphatic substituents.Conformational Plasticity of the Cell-Penetrating Peptide SAP As Revealed by Solid-State 19F-NMR and Circular Dichroism Spectroscopies.Delivering Structural Information on the Polar Face of Membrane-Active Peptides: (19) F-NMR Labels with a Cationic Side Chain.Design, Synthesis, and Application of an Optimized Monofluorinated Aliphatic Label for Peptide Studies by Solid-State (19) F NMR Spectroscopy.Stereochemical effects on the aggregation and biological properties of the fibril-forming peptide [KIGAKI]3 in membranes.Incorporation of cis- and trans-4,5-difluoromethanoprolines into polypeptides.The catalytic asymmetric α-benzylation of aldehydes.Conformationally Rigid Trifluoromethyl-Substituted α-Amino Acid Designed for Peptide Structure Analysis by Solid-State19F NMR SpectroscopyThe Most Twisted Amide: Structure and ReactionsEfficiently Photocontrollable or Not? Biological Activity of Photoisomerizable DiarylethenesFrontispiece: Efficiently Photocontrollable or Not? Biological Activity of Photoisomerizable DiarylethenesDesign and Synthesis of a Monofluoro-Substituted Aromatic Amino Acid as a Conformationally Restricted19F NMR Label for Membrane-Bound PeptidesA19F NMR Label to Substitute Polar Amino Acids in Peptides: A CF3-Substituted Analogue of Serine and ThreonineDesign, Synthesis, and Application of a Trifluoromethylated Phenylalanine Analogue as a Label to Study Peptides by Solid-State19F NMR SpectroscopyIncorporation of labile trans-4,5-difluoromethanoproline into a peptide as a stable label for 19F NMR structure analysisIncorporation of cis- and trans-4,5-Difluoromethanoprolines into PolypeptidesAn optimized protocol for the multigram synthesis of 3-(trifluoromethyl)bicyclo[1.1.1]pent-1-ylglycine (CF3-Bpg)Synthesis of a Conformationally Rigid Analogue of 2-Aminoadipic Acid Containing an 8-Azabicyclo[3.2.1]octane SkeletonA Convenient Route to Trifluoromethyl-Substituted Cyclopropane DerivativesEvaluating the amino acid CF3-bicyclopentylglycine as a new label for solid-state19F-NMR structure analysis of membrane-bound peptidesHighly reactive bis-cyclooctyne-modified diarylethene for SPAAC-mediated cross-linkingSynthesis of 7-azabicyclo[2.2.1]heptane-1,4-dicarboxylic acid, a rigid non-chiral analogue of 2-aminoadipic acidThe Most Reactive Amide As a Transition-State Mimic For cis–trans InterconversionPhosphorylation of 1,3-Di(N-alkyl)Azoles by Phosphorus(V) Acid Chlorides — a Route to Potential Haptens Derived from Phosphinic AcidsSilica with immobilized phosphinic acid-derivative for uranium extraction
P50
Q33769108-A0E4D11E-FE16-47F1-A127-1C033392AB42Q33972880-831970D7-885A-4C5E-AFA0-1D1CF205E55AQ34323636-B9CEA032-C2E4-4BF0-B931-6802509BF1CEQ34405548-106A9040-8AFD-49CC-AAA8-7688E86A6F98Q35052778-D6283F7E-2458-4691-9825-25B843D44D93Q42942823-4A4DD125-952C-47C6-9732-E9CB5D0D5E96Q43101892-1131C524-B60C-4CE1-8034-43E040EE387FQ43182297-FD78E962-0DAD-468A-9B34-741B975D711EQ44162084-C85A68FB-D217-4CFD-B2C5-8697C62271A4Q44256044-81A2FE16-66BB-4504-8716-35D399B61FA2Q44331214-ECA0DAA0-5CBE-403C-B120-B9A7116C97C5Q44587500-2DAC6002-DB53-46C3-886C-645BB19EB938Q45854622-15E81D3A-60B7-4E67-B4B0-676D117FD0B0Q46521506-E1681D29-A053-4136-869C-793A11796481Q46571666-519251CF-0B6B-4CFE-A0CC-D87DD6B84D12Q46835840-5195BB41-4DDD-4CD6-B526-D336645CE973Q48285606-62F882E5-DE10-455E-BB2E-427C2C733CE5Q48288601-2ABC60F9-5D54-4465-B28E-FCC1F029E2CDQ48319286-57B97146-F778-4EEA-8697-76B484A9C3B7Q51012628-03588E4F-19D8-49C5-97CF-32345C9CB133Q53142774-C6F5A23C-6AEF-4865-832F-904073C89E5BQ54541415-0C9984B9-7242-48EE-92FF-35DE606EE818Q55998859-BEB5175F-0707-4B89-8EB1-CCE636D82791Q56477089-76723B82-1410-481C-A3E9-25586690CA2FQ57528264-680E99C8-F8AA-48D2-9DF3-8E782CD198C4Q57528267-D1421E25-948B-444C-BA1E-89314627D267Q57528325-3C4F7A3F-72BF-4CA8-9823-AD3177E10843Q57528340-F5B4201A-2CD8-4B19-AE06-33AB7F75C2C4Q57528343-9308253A-7707-433A-BE6D-69AACC5B1D68Q57528345-2DE3E84F-5538-494E-AC82-094AC18F1757Q57528360-FECA6712-F5F0-4021-AFB4-21720ECB65B9Q57528431-1DBB2025-F97B-4873-97F1-63B33DFCAC53Q57528471-7DBD2ABB-88F1-49BF-A033-E8C29F209E8BQ57528473-2826C033-B570-4694-875A-86A7263EFE8EQ57528485-F0446F1E-5CDE-41AC-AD5F-23A9D25A7D44Q58496679-F0D22EA3-B39A-4E83-89C2-B1B2ABBCF322Q59866722-FE1FB136-C599-4D7A-8E25-295165BD523FQ60308655-ABEF3100-8B2C-48AC-9E57-45591985532CQ60308656-9F9B37E8-E38B-47F4-BD20-40FEFCBF89D2Q60308657-D5BC35ED-04C1-4576-9DD8-E2F03C6A546F
P50
description
Russisch onderzoeker
@nl
hulumtues
@sq
researcher
@en
taighdeoir
@ga
հետազոտող
@hy
name
Igor V. Komarov
@ast
Igor V. Komarov
@en
Igor V. Komarov
@es
Igor V. Komarov
@nl
Igor V. Komarov
@sl
Игорь В. Комаров
@ru
type
label
Igor V. Komarov
@ast
Igor V. Komarov
@en
Igor V. Komarov
@es
Igor V. Komarov
@nl
Igor V. Komarov
@sl
Игорь В. Комаров
@ru
altLabel
Игорь Комаров
@ru
Комаров, Игорь
@ru
prefLabel
Igor V. Komarov
@ast
Igor V. Komarov
@en
Igor V. Komarov
@es
Igor V. Komarov
@nl
Igor V. Komarov
@sl
Игорь В. Комаров
@ru
P735
P1053
C-5467-2015
P106
P1153
7004891576
P21
P31
P3829
P496
0000-0002-7908-9145