المؤلفون: Rodríguez Serrat, Mònica

المساهمون: University/Department: Universitat de Girona. Departament de Química, University/Department: Universitat de Girona. Institut de Química Computacional i Catàlisi

Thesis Advisors: Costas Salgueiro, Miquel, Hernán-Gómez Robledo, Alberto

المصدر: TDX (Tesis Doctorals en Xarxa)

مصطلحات موضوعية: Organometallics, Química organometàl·lica, Química organometálica, Carbene transfer, Transferència de carbè, Transferencia de carbeno, Catalysis, Catàlisi, Catálisis, Transition metals, Metalls de transició, Metales de transición, C-H functionalization, Funcionalització d'enllaços C-H, Funcionalización de enlaces C-H, N-heterocyclic carbene, Carbè N-heterocíclic, Carbeno N-heterocíclico

وصف الملف: application/pdf

URL الوصول: http://hdl.handle.net/10803/668829

المؤلفون: Sabeña Vila, Gerard

المساهمون: University/Department: Universitat de Girona. Departament de Química

Thesis Advisors: Costas Salgueiro, Miquel, Lloret Fillol, Julio

المصدر: TDX (Tesis Doctorals en Xarxa)

مصطلحات موضوعية: Iron-oxo, Ferro-oxo, Hierro-oxo, Iron-imido, Ferro-imido, Hierro-imido, Iron-nitrido, Ferro-nitrè, Hierro-nitrido, Iron-carbene, Ferro-carbè, Hierro-carbeno, Arene functionalisation, Funcionalització d'arens, Funcionalización de arenos, Carbene transfer, Transferència de carbè, Transferencia de carbeno

وصف الملف: application/pdf

URL الوصول: http://hdl.handle.net/10803/406145

المؤلفون: Mingyao Huang, Wenjing Shi, Lu Li

المصدر: Symmetry, Vol 16, Iss 9, p 1171 (2024)

مصطلحات موضوعية: asymmetric catalysis, carbenes, heteratom, carbene transfer reactions, Mathematics, QA1-939

Relation: https://www.mdpi.com/2073-8994/16/9/1171; https://doaj.org/toc/2073-8994; https://doaj.org/article/89df980561034d168b523eb2c52f0506

الاتاحة: https://doi.org/10.3390/sym16091171
https://doaj.org/article/89df980561034d168b523eb2c52f0506

المؤلفون: Perez, Pedro J., Pizarro, Juan Diego, Moran-Gonzalo, Lucia, Gonzalez-Fernandez, Ivan, Maseras, Feliu, Romero-Fructos, Manuel

مصطلحات موضوعية: Indole functionalization, carbene transfer, selective C- H functionalization, N- H bond, donoracceptor, 23 Química

Relation: Diego Pizarro, J., Morán‐González, L., González‐Fernández, I., Maseras, F., Fructos, M. R., & Pérez, P. J. (2023). Selective C−H Bond Functionalization of Unprotected Indoles by Donor‐Acceptor Carbene Insertion. In Advanced Synthesis & Catalysis (Vol. 366, Issue 4, pp. 844–851). Wiley. https://doi.org/10.1002/adsc.202300252; 1615-4169 (electrónico); https://hdl.handle.net/10272/23372

الاتاحة: https://hdl.handle.net/10272/23372
https://doi.org/10.1002/adsc.202300252

المؤلفون: Matamoros Recio, Alejandra, Alonso Rueda, Elia, Borrego, Elena, Caballero Bevia, Ana, Pérez Romero, Pedro José, Martín Santamaria, Sonsoles

مصطلحات موضوعية: Carbene Transfer in Micelles, Methane Functionalization, Micellar Catalysis, Molecular Dynamics Simulations, Organometallic Catalysis, 23 Química

Relation: Publisher's version; Matamoros‐Recio, A., Alonso‐Rueda, E., Borrego, E., Caballero, A., Pérez, P. J., & Martín‐Santamaría, S. (2024). Molecular Dynamic Simulations of Aqueous Micellar Organometallic Catalysis: Methane Functionalization as a Case Study. In Angewandte Chemie International Edition (Vol. 63, Issue 8). Wiley. https://doi.org/10.1002/anie.202314773; 1521-3773 (electrónico); https://hdl.handle.net/10272/23371

الاتاحة: https://hdl.handle.net/10272/23371
https://doi.org/10.1002/anie.202314773

المؤلفون: Roose, Thomas R., Preschel, H. Daniel, Mayo Tejedor, Helena, Roozee, Jasper C., Hamlin, Trevor A., Maes, Bert U.W., Ruijter, Eelco, Orru, Romano V.A.

المصدر: Roose , T R , Preschel , H D , Mayo Tejedor , H , Roozee , J C , Hamlin , T A , Maes , B U W , Ruijter , E & Orru , R V A 2023 , ' Iron-Catalysed Carbene Transfer to Isocyanides as a Platform for Heterocycle Synthesis ' , Chemistry - A European Journal , vol. 29 , no. 9 , e202203074 . https://doi.org/10.1002/chem.202203074

مصطلحات موضوعية: carbene transfer, Hieber anion, iron catalysis, isocyanide, ketenimine, /dk/atira/pure/sustainabledevelopmentgoals/clean_water_and_sanitation, name=SDG 6 - Clean Water and Sanitation

الاتاحة: https://research.vu.nl/en/publications/6749de18-37ea-4767-8de7-00714975c05b
https://doi.org/10.1002/chem.202203074
https://hdl.handle.net/1871.1/6749de18-37ea-4767-8de7-00714975c05b
http://www.scopus.com/inward/record.url?scp=85144349274&partnerID=8YFLogxK
http://www.scopus.com/inward/citedby.url?scp=85144349274&partnerID=8YFLogxK

المؤلفون: Jason R. Combs, David S. Carter, Fengyi Gu, Xiaokang Jin, Connor M. Martin, Elizabeth S. Resendiz, David L. Van Vranken

مصطلحات موضوعية: Biochemistry, Microbiology, Genetics, Evolutionary Biology, Immunology, Infectious Diseases, Computational Biology, Chemical Sciences not elsewhere classified, punching quaternary centers, monocyclic benzene homologue, gives good results, generating sulfonium ylides, catalyzes carbene transfer, benzofuran ring systems, also competent substrates, reaction works well, 4 , yields improve, arylmethyl thioethers, aryl thioethers, aromatic rings, alkyl thioethers

Relation: https://figshare.com/articles/journal_contribution/Rhodium_II_-Catalyzed_Hinsberg_Dearomatization_Using_Trimethylsilyldiazomethane/24498581

الاتاحة: https://doi.org/10.1021/acs.orglett.3c03130.s002
https://figshare.com/articles/journal_contribution/Rhodium_II_-Catalyzed_Hinsberg_Dearomatization_Using_Trimethylsilyldiazomethane/24498581

المؤلفون: Kaveh Farshadfar, Arsalan Hashemi, Reza Khakpour, Kari Laasonen

مصطلحات موضوعية: Biophysics, Biochemistry, Space Science, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, lower energy barrier, activation energy required, many chemical transformations, carbene transfer reactions, vacant p orbital, combined machine learning, 2 , carbene lone pair, negative n charge, negative charge, machine learning, lone pair, chemical features, carbene precursors, carbene generation, carbene formation, carbene carbon, weak interaction, terminal nitrogen, synthetic chemistry, substituents located, results suggest, molecular engineering, highly dependent, functionalization procedures

Relation: https://figshare.com/articles/journal_contribution/Kinetics_of_N_sub_2_sub_Release_from_Diazo_Compounds_A_Combined_Machine_Learning-Density_Functional_Theory_Study/24844038

الاتاحة: https://doi.org/10.1021/acsomega.3c07367.s001
https://figshare.com/articles/journal_contribution/Kinetics_of_N_sub_2_sub_Release_from_Diazo_Compounds_A_Combined_Machine_Learning-Density_Functional_Theory_Study/24844038

المؤلفون: Martínez-Laguna, Jonathan, Mollar-Cuni, Andrés, Ventura Espinosa, David, Martín, Santiago, Caballero, Ana, Mata, José A., Pérez, Pedro J.

مصطلحات موضوعية: Gold nanoparticles, Carbene transfer reactions, Au NPs, C-H bonds functionalization, Graphene, Gold catalysis, Reduced graphene oxide, Heterogeneous catalysis

وصف الملف: application/pdf

Relation: Publisher's version; Sí; XXXVIII Reunión Bienal de la Real Sociedad Española de Química (2022); http://hdl.handle.net/10261/284725

الاتاحة: http://hdl.handle.net/10261/284725

المؤلفون: Mary G. Siriboe, Rudi Fasan

المصدر: Bulletin of Japan Society of Coordination Chemistry. 2022, 80:4

المؤلفون: Xinkun Ren (3116727), Bo M. Couture (14289661), Ningyu Liu (6441577), Manjinder S. Lall (1936498), Jeffrey T. Kohrt (2022559), Rudi Fasan (1307055)

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Molecular Biology, Biotechnology, Computational Biology, Chemical Sciences not elsewhere classified, using engineered variants, offer new opportunities, cytochrome p450 cyp119, cyclic amine substrate, considerable synthetic value, direct asymmetric α, carbene transfer reaction, based biocatalytic strategy, 270 ton ), high catalytic activity, enable enantioselective α, >- heterocycles via, enantioselective α, >- heterocycles, carbene donor, biocatalytic approach, 350 ton, high yields, high stereoselectivity, enantioselective single, work provides, two strategies, tunable method

Relation: https://figshare.com/articles/journal_contribution/Enantioselective_Single_and_Dual_C_H_Bond_Functionalization_of_Cyclic_Amines_via_Enzymatic_Carbene_Transfer/21763963

الاتاحة: https://doi.org/10.1021/jacs.2c10775.s001

المؤلفون: María Álvarez (3951581), Francisco Molina (4028669), Pedro J. Pérez (1621264)

مصطلحات موضوعية: Biophysics, Biochemistry, Cell Biology, Genetics, Neuroscience, Biotechnology, Cancer, Mental Health, Physical Sciences not elsewhere classified, silver catalysis control, directing groups ), via carbene transfer, linear alkanes c, 2 , controlled regioselective functionalization, linear alkanes, controlled strategy, unprecedented level, secondary sites, mainly governed, large differences, electronic properties, diazo reagent, diazo compounds, alternative approach

Relation: https://figshare.com/articles/journal_contribution/Carbene-Controlled_Regioselective_Functionalization_of_Linear_Alkanes_under_Silver_Catalysis/21720173

الاتاحة: https://doi.org/10.1021/jacs.2c11707.s001

Thesis Advisors: Rodríguez Belderraín, Tomás, Romero Fructos-Vázquez, Manuel, Universidad de Huelva. Departamento de Química “Profesor José Carlos Vílchez Martín”

مصطلحات موضوعية: Catalizadores, NHC, Níquel, Paladio, Acoplamiento cruzado, Transferencia de carbenos, Nickel, Palladium, Cross-coupling, Carbene transfer

URL الوصول: http://hdl.handle.net/10272/14674

المؤلفون: Pujol, Manon, Degeilh, Lison, Sauty de Chalon, Thibault, Réglier, Marius, Simaan, A. Jalila, Decroos, Christophe

المساهمون: Institut des Sciences Moléculaires de Marseille (ISM2), Aix Marseille Université (AMU)-École Centrale de Marseille (ECM)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), ANR-18-CE07-0003,Abiozyme,Ingénierie de nouvelles métalloenzymes pour la catalyse abiologique(2018)

المصدر: ISSN: 0162-0134 ; Journal of Inorganic Biochemistry ; https://hal.science/hal-04668325 ; Journal of Inorganic Biochemistry, 2024, 260, pp.112688. ⟨10.1016/j.jinorgbio.2024.112688⟩.

مصطلحات موضوعية: artificial heme enzyme, sigmatropic rearrangement, carbene transfer, ylides, carbenoids, [CHIM.ORGA]Chemical Sciences/Organic chemistry, [CHIM.CATA]Chemical Sciences/Catalysis

Relation: hal-04668325; https://hal.science/hal-04668325; https://hal.science/hal-04668325/document; https://hal.science/hal-04668325/file/SommeletHauser_JInorgBiochem_R1.pdf

الاتاحة: https://hal.science/hal-04668325
https://hal.science/hal-04668325/document
https://hal.science/hal-04668325/file/SommeletHauser_JInorgBiochem_R1.pdf
https://doi.org/10.1016/j.jinorgbio.2024.112688

المؤلفون: Roelfes, Gerard

المصدر: Roelfes , G 2021 , ' Repurposed and artificial heme enzymes for cyclopropanation reactions ' , Journal of Inorganic Biochemistry , vol. 222 , 111523 . https://doi.org/10.1016/j.jinorgbio.2021.111523

مصطلحات موضوعية: Heme enzymes, Cyclopropanation, Repurposed heme enzymes, Artificial heme enzymes, Carbene transfer, Metallo-carbenoid

وصف الملف: application/pdf

الاتاحة: https://hdl.handle.net/11370/6fb31671-6fa7-4229-b203-05ed1047e132
https://research.rug.nl/en/publications/6fb31671-6fa7-4229-b203-05ed1047e132
https://doi.org/10.1016/j.jinorgbio.2021.111523
https://pure.rug.nl/ws/files/175413360/1_s2.0_S0162013421001707_main.pdf

المؤلفون: Xinyu Zhang (14029), Chunqi Tian (11047959), Zhanjing Wang (11047962), Paramasivam Sivaguru (4266193), Steven P. Nolan (1489711), Xihe Bi (1457866)

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Microbiology, Genetics, Biotechnology, Sociology, Immunology, Infectious Diseases, Virology, Chemical Sciences not elsewhere classified, enantioselectivity, small-ring products feature, triftosylhydrazone, theory calculations, group tolerance, fluoroalkyl chiral quaternary carbo., sulfonylhydrazone, chiral rhodium catalyst, fluoroalkyl-aryl ketone N, Decomposable Diazo Surrogates, carbene transfer reactions, fluoroalkylated cyclopropenes, release reactive diazo compounds, alkyne, cyclopropenation reaction, Chiral Fluoroalkyl Cyclopropenes

Relation: https://figshare.com/articles/journal_contribution/Fluoroalkyl_i_N_i_Triftosylhydrazones_as_Easily_Decomposable_Diazo_Surrogates_for_Asymmetric_2_1_Cycloaddition_Synthesis_of_Chiral_Fluoroalkyl_Cyclopropenes_and_Cyclopropanes/14879496

الاتاحة: https://doi.org/10.1021/acscatal.1c01483.s002

المؤلفون: Marc Garcia-Borràs (1530844), S. B. Jennifer Kan (10720965), Russell D. Lewis (3116877), Allison Tang (10720968), Gonzalo Jimenez-Osés (10720971), Frances H. Arnold (131156), K. N. Houk (1247004)

مصطلحات موضوعية: Biophysics, Biochemistry, Genetics, Biotechnology, Inorganic Chemistry, Infectious Diseases, Computational Biology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, cytochrome c heme protein, dynamic, chemical transformations, loop conformation, Cytochrome c Catalyzed Carbene Transfer, protein structure, substrate access, High chemoselectivity, carbene insertion, Si, protein loop, residues computationally, bond

Relation: https://figshare.com/articles/journal_contribution/Origin_and_Control_of_Chemoselectivity_in_Cytochrome_i_c_i_Catalyzed_Carbene_Transfer_into_Si_H_and_N_H_bonds/14509182

الاتاحة: https://doi.org/10.1021/jacs.1c02146.s001

المؤلفون: Hamada S. A. Mandour, Yoko Nakagawa, Masaya Tone, Hayato Inoue, Nansalmaa Otog, Ikuhide Fujisawa, Soda Chanthamath, Seiji Iwasa

المصدر: Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 357-363 (2019)

مصطلحات موضوعية: asymmetric synthesis, carbene transfer, cyclopropanation, diazoester, intramolecular diazoamide, Ru(II)-Pheox, water-soluble catalyst, Weinreb amide, Science, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1860-5397

URL الوصول: https://doaj.org/article/f47030cdedfd40c0bf91e708c5d46e5d

المؤلفون: Silvia G. Rull, Andrea Olmos, Pedro J. Pérez

المصدر: Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 67-71 (2019)

مصطلحات موضوعية: carbene transfer, cyclopropane, cyclopropylcarboxylate, ethylene cyclopropanation, ethyl diazoacetate, gold catalysis, Science, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1860-5397

URL الوصول: https://doaj.org/article/2c7ef6e0fd8649bba1a2ba1323c55a43

المؤلفون: Frances H. Arnold

المصدر: Molecular Frontiers Journal, Vol 2, Iss 1, Pp 9-18 (2018)

مصطلحات موضوعية: Enzyme Evolution, Directed Evolution, Carbene Transfer, Organosilicon, Biocatalysis, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2529-7325; https://doaj.org/toc/2529-7333

URL الوصول: https://doaj.org/article/a2ea8ca3dc25467c8d56b10c3853b609