المؤلفون: Longfei Yan, Guoyu Wang, Dongsheng Xiang, Yu Zhang, Weiping Deng

المصدر: Carbon Neutrality, Vol 3, Iss 1, Pp 1-23 (2024)

مصطلحات موضوعية: Biomass, Bio-platform molecules, Reductive amination, N-containing chemicals, Energy industries. Energy policy. Fuel trade, HD9502-9502.5, Renewable energy sources, TJ807-830

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2788-8614; https://doaj.org/toc/2731-3948

URL الوصول: https://doaj.org/article/6b9a6d8de8b940d6bd2b50439107035f

المؤلفون: Pengcheng Xie, Jin Lan, Jingshuan Zhou, Zhun Hu, Jiandong Cui, Ge Qu, Bo Yuan, Zhoutong Sun

المصدر: Bioresources and Bioprocessing, Vol 11, Iss 1, Pp 1-11 (2024)

مصطلحات موضوعية: Continuous flow, Asymmetric reductive amination, Amine dehydrogenases, Co-immobilization, Packed bed reactor, Technology, Chemical technology, TP1-1185, Biotechnology, TP248.13-248.65

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2197-4365

URL الوصول: https://doaj.org/article/044233c248db431f96aa6a0d4e1dbecb

المؤلفون: Xiufang Ding, Yue Wang, Sida Zhang, Ruihua Zhang, Dong Chen, Changcai Liu, Jianfu Xu, Long Chen

المصدر: Amino Acids, Vol 56, Iss 1, Pp 1-11 (2024)

مصطلحات موضوعية: Reductive amination, MVIIA, Conotoxin, Modification, Self-assembly, Biochemistry, QD415-436, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1438-2199

URL الوصول: https://doaj.org/article/e5dad2a2a44c4d12aaf9e62bd0a8b9ac

المؤلفون: Jian Yang, Jia Zhang, Enrico Benassi, Xuemei Li, Hailong Liu, Weiguo Fang, Junying Tian, Chungu Xia, Zhiwei Huang

المصدر: Green Chemical Engineering, Vol 5, Iss 1, Pp 119-131 (2024)

مصطلحات موضوعية: NiCo bimetallic catalysts, Layered double hydroxide, Reductive amination, Amino alcohol, Quantum chemical calculations, Chemical engineering, TP155-156, Biochemistry, QD415-436

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2666952823000043; https://doaj.org/toc/2666-9528

URL الوصول: https://doaj.org/article/78db5fd73abd4cd2bdd4396ec9e20148

المؤلفون: Anne Zenner, Johannes Steinmetzer, Nico Ueberschaar, Martin Freesmeyer, Wolfgang Weigand, Julia Greiser

المصدر: Royal Society Open Science, Vol 11, Iss 7 (2024)

مصطلحات موضوعية: 1,4-diazepane-6-amine, reductive amination, synthesis investigation, Science

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2054-5703

URL الوصول: https://doaj.org/article/909b276084ef4b8783f99a251b503bc2

المؤلفون: Sooyoung Kim, Jae-Hwan Kwak, Jae-Kyung Jung, Soonsil Hyun

المصدر: Journal of Analytical Science and Technology, Vol 15, Iss 1, Pp 1-9 (2024)

مصطلحات موضوعية: 14C-labeling, Reductive amination, Antibody, Microdosing, 14C-formaldehyde, Chemistry, QD1-999, Analytical chemistry, QD71-142

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2093-3371

URL الوصول: https://doaj.org/article/0393b4f6cdc644e29c065204b171a84b

المؤلفون: Huang, Yu-Ping, Robinson, Randall C, Barile, Daniela

المصدر: Journal of food and drug analysis. 30(1)

مصطلحات موضوعية: Oligosaccharides, Raffinose, Electrophoresis, Capillary, Mass Spectrometry, Glycomics, Nutrition, In-source fragmentation, Oligosaccharide degradation, Raffinose-family oligosaccharides, Reductive amination, Sialylated oligosaccharides, Food Sciences, Analytical Chemistry

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/28f119s2

المؤلفون: Boulos, Joseph, Goc, Firat, Vandenbrouck, Tom, Perret, Noémie, Dhainaut, Jérémy, Royer, Sébastien, Rataboul, Franck

المساهمون: Institut de recherches sur la catalyse et l'environnement de Lyon (IRCELYON), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Université d'Artois (UA)-Centrale Lille-Institut de Chimie - CNRS Chimie (INC-CNRS)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)

المصدر: ISSN: 1864-5631.

مصطلحات موضوعية: 2-Aminopropanol Ammonia Cellulose Heterogeneous catalysis Reductive amination, 2-Aminopropanol, Ammonia, Cellulose, Heterogeneous catalysis, Reductive amination, [CHIM]Chemical Sciences

الاتاحة: https://hal.science/hal-04728826
https://hal.science/hal-04728826v1/document
https://hal.science/hal-04728826v1/file/Manuscript%20accepted%20for%20publication.pdf
https://doi.org/10.1002/cssc.202400540

المؤلفون: Artur Maier, Tanja Knaus, Francesco G. Mutti, Dirk Tischler

مصطلحات موضوعية: Biochemistry, Microbiology, Molecular Biology, Biotechnology, Developmental Biology, Computational Biology, Biological Sciences not elsewhere classified, whole cell approach, unlocking catalytic diversity, altered binding conformation, asymmetric reductive amination, 2 , reductive amination, substrate binding, n <, reductive aminase, work broadens, various reactions, substrate specificity, silico docking, nadh regeneration, less effort, formate dehydrogenase, derivatives thereof, cofactors nadh, catalyzed cleavage, cascade set, candida boidinii, aspergillus oryzae, applied enzyme

Relation: https://figshare.com/articles/journal_contribution/Unlocking_Catalytic_Diversity_of_a_Formate_Dehydrogenase_Formamide_Activity_for_NADPH_Regeneration_and_Amine_Supply_for_Asymmetric_Reductive_Amination/25091702

الاتاحة: https://doi.org/10.1021/acscatal.3c05409.s001
https://figshare.com/articles/journal_contribution/Unlocking_Catalytic_Diversity_of_a_Formate_Dehydrogenase_Formamide_Activity_for_NADPH_Regeneration_and_Amine_Supply_for_Asymmetric_Reductive_Amination/25091702

المؤلفون: Joseph M. Phelps, Roopender Kumar, James D. Robinson, John C. K. Chu, Nils J. Flodén, Sarah Beaton, Matthew J. Gaunt

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Molecular Biology, Pharmacology, Biotechnology, Science Policy, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, order ” variant, halogen atom transfer, displayed scalability issues, certain substrate classes, carbonyl reductive amination, carbonyl alkylative amination, biologically active molecules, 10 μmol setup, improved reaction scope, current benchmark methods, containing compounds continue, competitive reductive amination, trialkyl tertiary amines, transformation enables robust, mediated caa reaction, extremely broad zinc, accessed via cra, branched alkylamine synthesis, reaction regime, relevant compounds, many methods

Relation: https://figshare.com/articles/journal_contribution/Multicomponent_Synthesis_of_Branched_Amines_via_a_Zinc-Mediated_Carbonyl_Alkylative_Amination_Reaction/25416622

الاتاحة: https://doi.org/10.1021/jacs.3c14037.s001

المؤلفون: Xiuzheng Zhuang, Jianguo Liu, Longlong Ma

المصدر: Green Energy & Environment, Vol 8, Iss 5, Pp 1358-1370 (2023)

مصطلحات موضوعية: Impregnation method, One-pot synthesis, Hydrochar-supported catalyst, Reductive amination, Renewable energy sources, TJ807-830, Ecology, QH540-549.5

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2468025722000127; https://doaj.org/toc/2468-0257

URL الوصول: https://doaj.org/article/fae9f841f3e74c4bb672afb44a317ff7

المؤلفون: Serhii M. Holovach, Kostiantyn P. Melnykov, Maryna S. Poluektova, Oleksandr B. Rozhenko, Oleksandr O. Grygorenko

المصدر: Журнал органічної та фармацевтичної хімії, Vol 21, Iss 3, Pp 11-16 (2023)

مصطلحات موضوعية: cycloalkanes, fluorine, levin’s anomeric amide, “nitrogen deletion”, reductive amination, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://ophcj.nuph.edu.ua/article/view/278321; https://doaj.org/toc/2308-8303; https://doaj.org/toc/2518-1548

URL الوصول: https://doaj.org/article/bfe5af5401754e4fb1553d16e7e2a3cb

المؤلفون: Ğarip Demir, Jarkko Valjakka, Ossi Turunen, Fatih Aktaş, Barış Binay

المصدر: Heliyon, Vol 10, Iss 5, Pp e26899- (2024)

مصطلحات موضوعية: Unnatural amino acids, L-Alanine dehydrogenase, Reductive amination mechanism, Active site modelling, Green synthesis, Science (General), Q1-390, Social sciences (General), H1-99

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S240584402402930X; https://doaj.org/toc/2405-8440

URL الوصول: https://doaj.org/article/0fbe17f5e92d431faea622abac15ab1d

المؤلفون: Pettersson Salom, Sofia Henriette

المساهمون: University/Department: Universitat Ramon Llull. IQS - Química Orgànica

Thesis Advisors: Teixidó Closa, Jordi

المصدر: TDX (Tesis Doctorals en Xarxa)

مصطلحات موضوعية: CXCR4 inhibitors, HIV, farmacóforo, QSAR, poliamines, aminación reductora, inhibidores de CXCR4, VIH, farmacòfor, aminació reductora, inhibidors de CXCR4, reductive amination, polyamines, pharmacophore, Química i Enginyeria Química

وصف الملف: application/pdf

URL الوصول: http://www.tdx.cat/TDX-1215109-152530
http://hdl.handle.net/10803/9298

المؤلفون: Clemente, Francesca, Martínez Bailén, Macarena, Matassini, Camilla, Morrone, Amelia, Falliano, Silvia, Caciotti, Anna, Paoli, Paolo, Goti, Andrea, Cardona, Francesca

المساهمون: Universidad de Sevilla. Departamento de Química Orgánica y Farmacéutica

مصطلحات موضوعية: Iminosugars, β-galactosidase inhibitors, GM1 gangliosidosis, GLB1, Pharmacological chaperones, Nitrones, Grignard reagents, Reductive amination

Relation: Molecules, 27 (13), 4008.; https://doi.org/10.3390/molecules27134008; https://idus.us.es/handle//11441/162194

الاتاحة: https://idus.us.es/handle//11441/162194

المؤلفون: Ma, Zhuang, Kuloor, Chakreshwara, Kreyenschulte, Carsten, Bartling, Stephan, Malina, Ondrej, Haumann, Michael, Menezes, Prashanth W., Zbořil, Radek, Beller, Matthias, Jagadeesh, Rajenahally V.

مصطلحات موضوعية: iron catalysis, single atoms, reductive amination, carbonyl compounds, amines, ddc:540

وصف الملف: 15 Seiten; application/pdf

الاتاحة: https://refubium.fu-berlin.de/handle/fub188/45295
https://doi.org/10.17169/refubium-45007
https://doi.org/10.1002/anie.202407859

المؤلفون: Maccow, Awilda, Kulyk, Hanna, Severac, Etienne, Morel, Sandrine, Moulis, Claire, Boissonnat, Guillaume, Remaud-Simeon, Magali, Guieysse, David

المساهمون: Toulouse Biotechnology Institute (TBI), Institut National des Sciences Appliquées - Toulouse (INSA Toulouse), Institut National des Sciences Appliquées (INSA)-Université de Toulouse (UT)-Institut National des Sciences Appliquées (INSA)-Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), MetaboHUB-MetaToul, MetaboHUB-Génopole Toulouse Midi-Pyrénées Auzeville (GENOTOUL), Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Ecole Nationale Vétérinaire de Toulouse (ENVT), Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Pili, This work was funded by the National Association for Research and Technology, France (ANRT) and PILI company (Bioreactive projet, 2018/1179) . We thank the PICT-ICEO facility dedicated to enzyme screening and discovery, and part of the Integrated Screening Platform of Toulouse (PICT, IBiSA) for providing access to equipment. PICT-ICEO is a member of IBISBA-FR (https://doi.org/10.15454/08BX-VJ91) , the French node of the European research infrastructure, IBISBA ( www.ibisba.eu)

المصدر: ISSN: 0144-8617.

مصطلحات موضوعية: Cellooligo, saccharides, Laccase, Oxidation, Reductive amination, Amino-chromophores, Enzymatic functionalization, grafting, cellobiose, methyl beta-D-cellobiose, TEMPO system, cellooligosaccharides, D-cellopentaose, mass spectrometry, LC-HRMS, MALDI-TOF, LC-UV-MS/MS, [SDE]Environmental Sciences, [CHIM]Chemical Sciences, [CHIM.MATE]Chemical Sciences/Material chemistry, [SDV]Life Sciences [q-bio]

Relation: info:eu-repo/semantics/altIdentifier/pmid/38763718; PUBMED: 38763718; WOS: 001238367900001

الاتاحة: https://hal.inrae.fr/hal-04669065
https://hal.inrae.fr/hal-04669065v1/document
https://hal.inrae.fr/hal-04669065v1/file/Maccow_etal_CarbohydratePolymers.pdf
https://doi.org/10.1016/j.carbpol.2024.122168

المؤلفون: Shenbagaraman Akshaya, Arputharaj Joseph Nathanael

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Pharmacology, Biotechnology, Ecology, Space Science, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, linear anionic polysaccharides, different sectors ranging, main functional groups, improve creaming ability, hydrophobically associated alginates, important chemical modifications, hydrophobically modified alginates, hydrophobically modified, chemical modifications, important role, carboxyl groups, water treatment, water emulsions, ugi reaction, thickening agents, sustained release, stabilize oil, reductive amination, produce gelling, predominantly hydrophilic, polymeric chain

Relation: https://figshare.com/articles/journal_contribution/A_Review_on_Hydrophobically_Associated_Alginates_Approaches_and_Applications/25016655

الاتاحة: https://doi.org/10.1021/acsomega.3c08619.s001
https://figshare.com/articles/journal_contribution/A_Review_on_Hydrophobically_Associated_Alginates_Approaches_and_Applications/25016655

المؤلفون: Gabriel Schäfer, Tony Fleischer, Aurélien Merot, Michael Erhardt, Boris Mathys

مصطلحات موضوعية: Biochemistry, Medicine, Developmental Biology, Infectious Diseases, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, scale chromatographic separation, oac )< sub, chiral enamine derived, novel telescoped sequence, also vastly improved, final reductive amination, methyl ester turned, 5 -( 2, novel stereoselective route, 3 , 1239 , cxcr7 antagonist act, cxcr7 antagonist, novel nabh, stereoselective route, ratio 5, methyl ester, generation route, stereoselective second, stereoselective reduction, trans <, situ <, cis <, ∼ 1

Relation: https://figshare.com/articles/journal_contribution/Development_of_a_Scalable_Stereoselective_Second-Generation_Route_for_CXCR7_Antagonist_ACT-1004-1239_via_Chiral_Enamine_Reduction_and_a_Novel_Telescoped_Sequence_of_Transesterification_i_cis_i_-to-_i_trans_i_Epimerization_and_Saponification/25043445

الاتاحة: https://doi.org/10.1021/acs.oprd.3c00446.s001
https://figshare.com/articles/journal_contribution/Development_of_a_Scalable_Stereoselective_Second-Generation_Route_for_CXCR7_Antagonist_ACT-1004-1239_via_Chiral_Enamine_Reduction_and_a_Novel_Telescoped_Sequence_of_Transesterification_i_cis_i_-to-_i_trans_i_Epimerization_and_Saponification/25043445

المؤلفون: Takaaki Yajima, Akito Katayama, Tsubasa Ito, Takuma Kawada, Kenya Yabushita, Toshihisa Yasuda, Takeshi Ohta, Takeaki Katayama, Noriyuki Utsumi, Yoshihito Kayaki, Shigeki Kuwata

مصطلحات موضوعية: Biochemistry, Microbiology, Genetics, Molecular Biology, Pharmacology, Biotechnology, Immunology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, satisfactory isolated yields, ir complexes bearing, excellent optical purities, asymmetric reductive amination, optically active 2, keto acids catalyzed, amino acids, >-( 2, subsequent elimination, orthoperiodic acid, n <, hydroxyethyl moiety, ee ), combined use, aminating agent, 20 examples

Relation: https://figshare.com/articles/journal_contribution/Asymmetric_Reductive_Amination_of_Keto_Acids_Using_Ir-Based_Hydrogen_Transfer_Catalysts_An_Access_to_Unprotected_Unnatural_Amino_Acids/25196737

الاتاحة: https://doi.org/10.1021/acs.orglett.3c04378.s001
https://figshare.com/articles/journal_contribution/Asymmetric_Reductive_Amination_of_Keto_Acids_Using_Ir-Based_Hydrogen_Transfer_Catalysts_An_Access_to_Unprotected_Unnatural_Amino_Acids/25196737