Absolute configurational assignments of secondary amines by CD-sensitive dimeric zinc porphyrin host.Synthesis and characterization of water-soluble free-base, zinc and copper porphyrin-oligonucleotide conjugates.Prof. Daniel W. armstrongAbsolute configuration of actinophyllic acid as determined through chiroptical data.Enantioselective synthesis of 3,4-chromanediones via asymmetric rearrangement of 3-allyloxyflavonesPorphyrins and metalloporphyrins: versatile circular dichroic reporter groups for structural studies.On the structure of endogenous ouabainPhysicochemical characterization of a ouabain isomer isolated from bovine hypothalamus.Combined synthetic/CD strategy for the preparation and configurational assignments of model acyclic 1,3-polyols with a 1,2-diol terminal.Application of electronic circular dichroism in configurational and conformational analysis of organic compounds.Three challenges toward the assignment of absolute configuration of gymnocin-BCharacterization of dihydro-A2PE: an intermediate in the A2E biosynthetic pathway.Probing molecular chirality by CD-sensitive dimeric metalloporphyrin hosts.Conformational aspects in the studies of organic compounds by electronic circular dichroism.Application of electronic circular dichroism in the study of supramolecular systems.Porphyrin substituted phosphoramidites: new building blocks for porphyrin-oligonucleotide syntheses.Absolute configurations of phytotoxic inuloxins B and C based on experimental and computational analysis of chiroptical properties.Search for an endogenous mammalian cardiotonic factor.Synthesis of 11-cis-locked bicyclo[5.1.0]octanyl retinal and an enantioselective binding to bovine opsin.Solution and biologically relevant conformations of enantiomeric 11-cis-locked cyclopropyl retinals.Theoretical analysis of the porphyrin-porphyrin exciton interaction in circular dichroism spectra of dimeric tetraarylporphyrins.Assignment of absolute configuration of a chiral phenyl-substituted dihydrofuroangelicin.Absolute stereochemistry of allylic alcohols, amines, and other ene moieties: a microscale cross metathesis/exciton chirality protocol.Absolute stereochemistry of dihydrofuroangelicins bearing C-8 substituted double bonds: a combined chemical/exciton chirality protocol.Trans-diaryl epoxides: asymmetric synthesis, ring-opening, and absolute configuration.Primary events in dim light vision: a chemical and spectroscopic approach toward understanding protein/chromophore interactions in rhodopsin.Determination of the absolute configuration of Anisotome irregular diterpenes: application of CD and NMR methods.Absolute configurational determination of an all-trans-retinal dimer isolated from photoreceptor outer segments.Detection of zinc ions by differential circularly polarized fluorescence excitation.Absolute configurations of fungal and plant metabolites by chiroptical methods. ORD, ECD, and VCD studies on phyllostin, scytolide, and oxysporone.An enantiomerically pure alleno-acetylenic macrocycle: synthesis and rationalization of its outstanding chiroptical response.Chiral induction from allenes into twisted 1,1,4,4-tetracyanobuta-1,3-dienes (TCBDs): conformational assignment by circular dichroism spectroscopy.Interactions of a tetraanionic porphyrin with DNA: from a Z-DNA sensor to a versatile supramolecular device.Reassessing the structure of pyranonigrin.Chiral sulfinates studied by optical rotation, ECD and VCD: the absolute configuration of a cruciferous phytoalexin brassicanal C.Chiral recognition of cyclic alpha-hydroxyketones by CD-sensitive zinc tetraphenylporphyrin tweezer.Theoretical simulation of the electronic circular dichroism spectrum of calicheamicin.Inherent chirality dominates the visible/near-ultraviolet CD spectrum of rhodopsin.Circular dichroism of heterochromophoric and partially regenerated purple membrane: search for exciton coupling.Complexation of Chiral Zinc-Porphyrin Tweezer with Achiral Diamines: Induction and Two-Step Inversion of Interporphyrin Helicity Monitored by ECD.
P50
Q29393859-9B57F90A-66B9-4694-8E5E-FB6482B62D6BQ30844295-C0683263-EB07-4A16-AF92-C8E141244D70Q33178706-78906215-E6C4-4ADE-81E5-F58DC0E750CFQ33409597-A2EAC478-3377-4283-90E4-68C9A7306178Q33596229-9D7F9226-7028-416F-BD48-E66D5AC11BF0Q33903147-D1DF2164-4A41-411F-8E50-6314A9BEC23FQ36378121-C31E842D-34C3-4080-BE79-131A788C9FF6Q36515871-77633191-69B0-4B45-A78B-C8FA2E937342Q36794772-D1F4755B-3A4B-4E93-8002-E71C167B458BQ36834095-80C2F96F-60FD-4FAA-84E2-027912DC94C8Q36858345-0D7EBE05-8F6E-4172-9028-B6913F785C4AQ36917117-33606E06-A0F4-4824-A854-3B916A5E8B4CQ37609976-F2A739EE-AFF0-4023-B7C6-63CE67BA3CE1Q37890260-6F4DED59-B454-4457-9FA1-439804567179Q38211609-28898CC3-171D-49A7-A79C-BA6DD460DFE7Q38329581-42DAEDAA-64B3-4E4A-BC0A-C19DD652A6C9Q39516390-405E95CB-4CEB-4E64-A824-332833799A9EQ41258966-7AEBE378-295A-48C1-8C0A-2E5D75E4501BQ43968187-F8C8BC43-3898-4FE5-9547-6975B875C8A8Q44032916-E0CA66C1-B97B-49D9-94F4-8B1DD4132AEFQ44481792-BD1C2D3D-7BF7-4D98-902B-A4229A3298D8Q44556669-C60C7346-35F9-4E06-B640-625C5A31EC30Q44571436-98A8E970-F3BF-46A4-AD86-FD72BB130421Q44737905-77B3801A-8ABF-4F9B-84A1-369089AD2A42Q44760800-83152C12-E94D-4C9A-914A-42E922137F68Q44837156-1A2E0C56-7968-4F20-988C-7F712DAA0298Q45004700-76AE0315-9560-4C19-9FE2-79A9AE2FC2A8Q45070126-49222D85-E949-42F8-ACEF-B545F2F13774Q45070554-2067402A-8331-4FBB-AC77-0AB80807BC1BQ45342349-F7835138-2754-4B46-B330-38B0762D1D07Q45966017-0E2BB53B-290C-467E-A3C5-ADFB53600A27Q46062878-8187898C-B7F0-44EF-A32B-CFD4449D022DQ46153695-F2BEE28A-452B-4747-8C99-D0CE2D132491Q46237620-3E7FDD1E-B349-4063-B435-B45B49F6CDBEQ46249888-8790CC83-6755-424E-A50B-B4BCD5FF0031Q46455993-F6E1EA11-DE16-4139-B8BB-F3A4CA35643EQ46623946-02683261-544C-4839-B15B-228AAEB1C919Q46639630-B37FCDFA-F12F-4888-AFA1-EE8E8A85467EQ46873136-9EC7D60B-384F-46E3-9DB8-21735135D151Q48045350-89FF22A5-6718-4DC2-A230-F0B550930662
P50
description
Professor of Chemistry
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Berova N
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Berova N. A.
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Berova N.
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Berova
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N Berova
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N D Berova
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N. Berova
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N. D. Berova
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Nina D Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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Nina Berova
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P69
P1006
P1015
P214
P244
P268
P269
P1006
P1015
P106
P1207
P1273
P166
P21
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0000 0001 1609 0328
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P7859
lccn-n93103535