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

العلاقة: 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/25091702Test

الإتاحة: https://doi.org/10.1021/acscatal.3c05409.s001Test
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/25091702Test

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

العلاقة: 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/25196737Test

الإتاحة: https://doi.org/10.1021/acs.orglett.3c04378.s001Test
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/25196737Test

المؤلفون: Yufeng Liu, Linzhou Wang, Yingjun Li, Baode Ma, Gen-Qiang Chen, Xumu Zhang

المصدر: Green Synthesis and Catalysis, Vol 3, Iss 3, Pp 298-301 (2022)

مصطلحات موضوعية: Asymmetric reductive amination, Chiral β-amino phosphine, Ruthenium-catalysed, Ammonium salt, Chemical technology, TP1-1185, Biochemistry, QD415-436

وصف الملف: electronic resource

العلاقة: http://www.sciencedirect.com/science/article/pii/S2666554922000679Test; https://doaj.org/toc/2666-5549Test

الوصول الحر: https://doaj.org/article/0f35fc06d93844359719be3782cfd030Test

المؤلفون: Zhenwei Wu (1408012), Hualing He (10144416), Minglei Chen (1977511), Linfei Zhu (14264306), Weitao Zheng (535228), Yang Cao (53545), Jon C. Antilla (1334853)

مصطلحات موضوعية: Biochemistry, Molecular Biology, Pharmacology, Biotechnology, Sociology, Immunology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, mild reaction conditions, chiral spinol borophosphates, asymmetric reductive amination, derived borophosphates, asymmetric synthesis, synthetic applicability, r <, pinacolborane catalyzed, excellent yields, established method, >)- fendiline

العلاقة: https://figshare.com/articles/journal_contribution/Asymmetric_Reductive_Amination_with_Pinacolborane_Catalyzed_by_Chiral_SPINOL_Borophosphates/21732215Test

الإتاحة: https://doi.org/10.1021/acs.orglett.2c03866.s001Test

المؤلفون: Dong-Hao Wang (11675106), Qi Chen (144168), Sai-Nan Yin (11675109), Xu-Wei Ding (11675112), Yu-Cong Zheng (5621252), Zhi Zhang (55283), Yu-Hui Zhang (2016115), Fei-Fei Chen (3383549), Jian-He Xu (1419973), Gao-Wei Zheng (2091172)

مصطلحات موضوعية: Biochemistry, Molecular Biology, Pharmacology, Biotechnology, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, widespread applications toward, several beneficial mutants, fine chemical industries, 50 ° c, engineered amine dehydrogenases, engineered amine dehydrogenase, optically pure amines, catalyzed reductive amination, asymmetric reductive amination, engineered enzymes m3, structurally diverse ketones, 2 u mg, reductive amination, engineered m3, chiral amines, three days, substrate scope, results demonstrate, promising method, promising biocatalysts, prochiral ketones, mutations improve, gram scale, gk <

العلاقة: https://figshare.com/articles/journal_contribution/Asymmetric_Reductive_Amination_of_Structurally_Diverse_Ketones_with_Ammonia_Using_a_Spectrum-Extended_Amine_Dehydrogenase/16980648Test

الإتاحة: https://doi.org/10.1021/acscatal.1c04324.s001Test

المؤلفون: Judith E. Farnberger, Elisabeth Lorenz, Nina Richter, Volker F. Wendisch, Wolfgang Kroutil

المصدر: Microbial Cell Factories, Vol 16, Iss 1, Pp 1-17 (2017)

مصطلحات موضوعية: Biocatalysis, Single-cell biotransformation, Escherichia coli, Asymmetric reductive amination, Transaminases, Chiral amines, Microbiology, QR1-502

وصف الملف: electronic resource

العلاقة: http://link.springer.com/article/10.1186/s12934-017-0750-5Test; https://doaj.org/toc/1475-2859Test

الوصول الحر: https://doaj.org/article/c63de272235d46698fbe306f243d0428Test

المؤلفون: Guorui Gao, Shaozhi Du, Yang Yang, Xue Lei, Haizhou Huang, Mingxin Chang

المصدر: Molecules; Volume 23; Issue 9; Pages: 2207

مصطلحات موضوعية: Alzheimer’s syndrome, rivastigmine, asymmetric reductive amination, asymmetric catalysis, phosphoramidite ligands

جغرافية الموضوع: agris

وصف الملف: application/pdf

العلاقة: Organic Chemistry; https://dx.doi.org/10.3390/molecules23092207Test

الإتاحة: https://doi.org/10.3390/molecules23092207Test

المؤلفون: Xu, Zefei, Yao, Peiyuan, Sheng, Xiang, Li, Jinlong, Li, Jianjiong, Yu, Shanshan, Feng, Jinhui, Wu, Qiaqing, Zhu, Dunming

المصدر: ACS Catalysis. 10(15):8780-8787

مصطلحات موضوعية: imine reductase, intramolecular asymmetric reductive amination, chiral amine, 4-diazepane, Suvorexant

وصف الملف: print

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-185400Test

المؤلفون: Philippe Kalck, Anton Cunillera, Carmen Claver, Martine Urrutigoïty, Cyril Godard

المساهمون: Departament de Química Física i Inorganica, Universitat Rovira i Virgili, Universitat Rovira i Virgili, Laboratoire de chimie de coordination (LCC), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie de Toulouse (ICT-FR 2599), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Alfredo Ricci, Luca Bernardi

المصدر: Methodologies in Amine Synthesis
Methodologies in Amine Synthesis: Challenges and Applications
Alfredo Ricci; Luca Bernardi. Methodologies in Amine Synthesis: Challenges and Applications, Wiley-VCH, pp.155-185, 2021, 9783527347391. ⟨10.1002/9783527826186.ch5⟩

مصطلحات موضوعية: Asymmetric hydroaminoalkylation, 010405 organic chemistry, Chemistry, Asymmetric hydroamination, 010402 general chemistry, Hydroaminomethylation, 01 natural sciences, 0104 chemical sciences, Catalysis, Metal-catalyzed reactions, Transition metal, Early metal to noble metal catalysts, Polymer chemistry, Asymmetric reductive amination, [CHIM.COOR]Chemical Sciences/Coordination chemistry, Chiral amines

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13a151f1f5310e248d710be8911b49d3Test
https://doi.org/10.1002/9783527826186.ch5Test

المؤلفون: Cunillera, Anton, Claver, Carmen, Godard, Cyril, Urrutigoity, Martine, Kalck, Philippe

المساهمون: Departament de Química Física i Inorganica, Universitat Rovira i Virgili, Universitat Rovira i Virgili, Laboratoire de chimie de coordination (LCC), Institut de Chimie de Toulouse (ICT), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS), Alfredo Ricci, Luca Bernardi

المصدر: Methodologies in Amine Synthesis: Challenges and Applications ; https://hal.science/hal-03241440Test ; Alfredo Ricci; Luca Bernardi. Methodologies in Amine Synthesis: Challenges and Applications, Wiley-VCH, pp.155-185, 2021, 9783527347391. ⟨10.1002/9783527826186.ch5⟩ ; https://onlinelibrary.wiley.com/doi/abs/10.1002/9783527826186.ch5Test

مصطلحات موضوعية: Chiral amines, Metal-catalyzed reactions, Asymmetric reductive amination, Asymmetric hydroamination, Asymmetric hydroaminoalkylation, Hydroaminomethylation, Early metal to noble metal catalysts, [CHIM.COOR]Chemical Sciences/Coordination chemistry

العلاقة: hal-03241440; https://hal.science/hal-03241440Test

الإتاحة: https://doi.org/10.1002/9783527826186.ch5Test
https://hal.science/hal-03241440Test