Category:Elena_BoldyrevaJelena_Wladimirowna_BoldyrewaElena_Boldyreva%D0%91%D0%BE%D0%BB%D0%B4%D1%8B%D1%80%D0%B5%D0%B2%D0%B0,_%D0%95%D0%BB%D0%B5%D0%BD%D0%B0_%D0%92%D0%BB%D0%B0%D0%B4%D0%B8%D0%BC%D0%B8%D1%80%D0%BE%D0%B2%D0%BD%D0%B0Jelena_Vladimirovna_Boldireva%D0%91%D0%BE%D0%BB%D0%B4%D0%B8%D1%80%D1%94%D0%B2%D0%B0_%D0%9E%D0%BB%D0%B5%D0%BD%D0%B0_%D0%92%D0%BE%D0%BB%D0%BE%D0%B4%D0%B8%D0%BC%D0%B8%D1%80%D1%96%D0%B2%D0%BD%D0%B0Q30249959
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Isoenergetic Polymorphism: The Puzzle of Tolazamide as a Case Study.Synthesis and structure-activity relationship of novel 1,4-diazabicyclo[2.2.2]octane derivatives as potent antimicrobial agents.Structural aspects of displacive transformations: what can optical microscopy contribute? Dehydration of Sm2(C2O4)3·10H2O as a case study.Breakthrough in the high-pressure structures of Ba based on full exploitation of aperiodic symmetry.Crystal structure of a 2:1 co-crystal of meloxicam with acetyl-endi-carb-oxy-lic acidTribenzoatobismuth(III): a new -polymorphDifferent effects of α- and γ-polymorphs of glycine on behavior of GC rats predisposed to catalepsy.Pressure-induced phase transitions in L-alanine, revisited.Two new structures in the glycine-oxalic acid system.Observation of subtle dynamic transitions by a combination of neutron scattering, X-ray diffraction and DSC: a case study of the monoclinic L-cysteine.A conformational polymorphic transition in the high-temperature epsilon-form of chlorpropamide on cooling: a new epsilon'-form.A new structure of a serotonin salt: comparison and conformational analysis of all known serotonin complexes.Dynamic single crystals: kinematic analysis of photoinduced crystal jumping (the photosalient effect).Structure-property relationships in the crystals of the smallest amino acid: an incoherent inelastic neutron scattering study of the glycine polymorphs.A urea complex of copper(II) hypophosphite at 293, 100 and 15 K.Dynamics and thermodynamics of crystalline polymorphs. 2. β-Glycine, analysis of variable-temperature atomic displacement parameters.Betaine 0.77-perhydrate 0.23-hydrate and common structural motifs in crystals of amino acid perhydrates.An interpretation of the "anomalous" changes in the low-wavenumber range of the Raman spectra of L-alanine crystals.Phase transitions in the crystals of L- and DL-cysteine on cooling: the role of the hydrogen-bond distortions and the side-chain motions. 2. DL-cysteine.Weak hydrogen bonds formed by thiol groups in N-acetyl-(L)-cysteine and their response to the crystal structure distortion on increasing pressure.Polymorphism of paracetamol: a new understanding of molecular flexibility through local methyl dynamics.DL-cysteinium semioxalate.Semi-maleate salts of L- and DL-serinium: the first example of chiral and racemic serinium salts with the same composition and stoichiometry.A high-pressure polymorph of chlorpropamide formed on hydrostatic compression of the α-form in saturated ethanol solution.Phase transitions in the crystals of L- and DL-cysteine on cooling: intermolecular hydrogen bonds distortions and the side-chain motions of thiol-groups. 1. L-cysteine.Pressure-induced phase transitions in crystalline L- and DL-cysteine.L-cysteinium semioxalate.Bis(DL-cysteinium) oxalate.Mechanochemistry of inorganic and organic systems: what is similar, what is different?Difference in the dynamic properties of chiral and racemic crystals of serine studied by Raman spectroscopy at 3-295 K.Crystal structure and proton conductivity of a new Cs3(H2PO4)(HPO4)·2H2O phase in the caesium di- and monohydrogen orthophosphate system.Large porous particles for respiratory drug delivery. Glycine-based formulations.Highlights from Faraday Discussion 170: challenges and opportunities of modern mechanochemistry, Montreal, Canada, 2014.New 1:1 and 2:1 salts in the `DL-norvaline-maleic acid' system as an example of assembling various crystal structures from similar supramolecular building blocks.Effects of the alpha- and gamma-polymorphs of glycine on the behavior of catalepsy prone rats.Anisotropic lattice softening near the structural phase transition in the thermosalient crystal 1,2,4,5-tetrabromobenzene.Ball-free mechanochemistry: in situ real-time monitoring of pharmaceutical co-crystal formation by resonant acoustic mixing.Different dynamics of chiral and racemic (L- and DL-) serine crystals: evidenced by incoherent inelastic neutron and Raman scattering.A new solvate of furosemide with dimethylacetamide.Studying weak inter-actions in crystals at high pressures: when hardware matters.
P50
Q33361425-58402721-7FD2-4789-8747-9EF0B24B7743Q38888034-A8720948-17D1-4060-B09F-238EEA3A7AB8Q41714370-9215C4BD-F6F9-49FC-AE5B-F08899FC9CC6Q42319286-4F4CD04F-EB88-49D2-8FFD-9695EDCF4141Q42358681-7897D912-ED8D-4BDF-A963-80636A711F2BQ42359596-A1BE06C4-3691-4EBA-B3D8-37CC093075F9Q42853624-677D9866-5F0E-435C-90EC-DDD015EB7895Q42970127-747F0338-76E6-48BD-A369-7B8156E24A82Q43044915-0C4E614F-2CB8-4EB5-BDA9-38F55D24908BQ43147478-B99A4682-3475-4C4C-8FB6-4FA2B72339D3Q43239200-2D742E6C-C1E2-49D3-A09B-483E4E8D8A81Q43449535-1AFA6C10-E612-4133-8C0B-72BD0168673BQ43623126-13E58B59-78B6-4ACB-ACA0-F9E7BC4EC06BQ43638873-7B884EB0-1CCE-4384-81E6-FB8DC3F6ECFAQ43666617-D676276B-7C0D-454C-BF42-EF8856089FC1Q43958896-98E1A3FC-09A0-4E22-931F-FC991CDDDCE1Q44599693-912D3A2B-16D3-45E2-885C-BA2639D47ADBQ44861107-60377D3B-ECAE-4624-98FA-22DEF2DDD0B2Q45056114-F980CC35-9BAE-49C8-93FD-89938270C3F4Q45218506-A2940B9D-F154-4C91-9AD8-6F0FBC0BE35DQ45894050-A3F982DC-84A6-4B99-9BE4-B7918F4B47BDQ46029591-674D95DE-6089-4F54-AC94-D5C2A16A6EFDQ46266728-5639BCC6-6A82-43AA-AD48-A47888973BF4Q46348346-95C7DE1A-6C54-4EE2-9BEA-2B34A54A7F46Q46366914-4FBBC40A-E91D-46BA-A13C-9E0268020419Q46508161-849ECAAA-F130-4FA9-B8F0-A8F4C37DBD8EQ46555149-B10B3F8F-908F-4CD6-A518-E6178C2E6A85Q46555179-98810A40-9307-4B87-A7B1-BE8575C3028CQ46819302-B2BEA893-5BD3-4AFC-BE3C-658147B14D7FQ46872147-B138DAFB-0DC3-480B-9168-525016EE3073Q47857372-DCB8FB66-6C74-4A06-80CF-2B21EE1E0B7CQ47899164-8380A795-9125-4BE7-9EA5-833C771ECC37Q50437907-D03F6AF8-3BAD-4868-ACCC-8596C6F6CDDEQ51064266-3E9F276A-2B3C-4ECA-9B6F-05B3B759BDB5Q51891332-F3917D68-DBFB-4FD5-8840-13FC168D5827Q52356269-78978767-5CC9-4A2B-901D-3B69D6FC097AQ52605798-2D312ABA-736F-400B-BA68-143A162EC48CQ52924032-27A89E5D-F11D-47D4-AAB0-8F561860C608Q53647716-AFC6FB49-ECBA-4E27-BEE9-EB82CAD7EC23Q55239840-3C6B418F-B6F6-486F-9606-A9858C0925D0
P50
description
Chimiste et professeur d'université soviétique
@fr
Russisch scheikundige
@nl
Soviet Russian solid state chemist and university lecturer
@en
ruska kemičarka
@sl
sowjetisch-russische Festkörperchemikerin und Hochschullehrerin
@de
російська хімікиня
@uk
كيميائية روسية
@ar
name
Elena Boldyreva
@en
Elena V. Boldyreva
@ast
Elena V. Boldyreva
@es
Elena Vladimirovna Boldyreva
@nl
Jelena Vladimirovna Boldireva
@sl
Jelena Wladimirowna Boldyrewa
@de
Jelena Wladimirowna Boldyrewa
@fr
Болдирєва Олена Володимирівна
@uk
Болдырева, Елена Владимировна
@ru
type
label
Elena Boldyreva
@en
Elena V. Boldyreva
@ast
Elena V. Boldyreva
@es
Elena Vladimirovna Boldyreva
@nl
Jelena Vladimirovna Boldireva
@sl
Jelena Wladimirowna Boldyrewa
@de
Jelena Wladimirowna Boldyrewa
@fr
Болдирєва Олена Володимирівна
@uk
Болдырева, Елена Владимировна
@ru
altLabel
Elena V. Boldyreva
@nl
Elena V. Boldyreva
@sl
Elena Vladimirovna Boldyreva
@de
Elena Vladimirovna Boldyreva
@en
Elena Vladimirovna Boldyreva
@fr
Болдырева, Елена Владимировна
@sq
prefLabel
Elena Boldyreva
@en
Elena V. Boldyreva
@ast
Elena V. Boldyreva
@es
Elena Vladimirovna Boldyreva
@nl
Jelena Vladimirovna Boldireva
@sl
Jelena Wladimirowna Boldyrewa
@de
Jelena Wladimirowna Boldyrewa
@fr
Болдирєва Олена Володимирівна
@uk
Болдырева, Елена Владимировна
@ru
P108
P214
P244
P108
P1153
7006629777
P1280
P19
P21
P214
P244
no00049462
P27
P31
P496
0000-0002-1401-2438
P5463
Boldyreva_Elena
P569
1961-02-04T00:00:00Z
P735
P7859
lccn-no00049462