المؤلفون: Li, Junhao, 1989, Tang, Yun, Li, Weihua, Tu, Yaoquan

المصدر: Biology Chemistry - A European Journal. 26(28):6214-6223

مصطلحات موضوعية: C-H hydroxylation, density functional calculations, hydroxylation, molecular modeling, P450, steroids, Kemi, Chemistry

وصف الملف: electronic

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-273352
https://doi.org/10.1002/chem.201905272
https://kth.diva-portal.org/smash/get/diva2:1430329/FULLTEXT02.pdf

المؤلفون: Ngoc Tan Cao, Ngoc Anh Nguyen, Thien-Kim Le, Gun Su Cha, Ki Deok Park, Chul-Ho Yun

المصدر: Catalysts; Volume 11; Issue 2; Pages: 267

مصطلحات موضوعية: biocatalyst, C-H hydroxylation, hederagenin, human CYP3A4, regioselective hydroxylation, oleanolic acid

وصف الملف: application/pdf

Relation: Biocatalysis; https://dx.doi.org/10.3390/catal11020267

الاتاحة: https://doi.org/10.3390/catal11020267

المؤلفون: Lv J., Zhao B., Yuan Y., Han Y., Shi Z.

المساهمون: Lv J., Zhao B., Yuan Y., Han Y., Shi Z.

مصطلحات موضوعية: Boron-mediated, C-H Hydroxylation

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000571382100001; volume:11; firstpage:1; lastpage:8; numberofpages:8; journal:NATURE COMMUNICATIONS; https://hdl.handle.net/11585/913392; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85081755499; https://www.nature.com/articles/s41467-020-15207-x#rightslink

الاتاحة: https://hdl.handle.net/11585/913392
https://doi.org/10.1038/s41467-020-15207-x
https://www.nature.com/articles/s41467-020-15207-x#rightslink

المؤلفون: Hans Renata (5329238), Emily Shimizu (10294828), Christian Zwick (7275336)

مصطلحات موضوعية: Natural Products, Biocatalysis, amino acid hydroxylation, C–H hydroxylation, non-heme oxygenase, non-ribosomal peptide

Relation: https://figshare.com/articles/preprint/Regiodivergent_Biocatalytic_Hydroxylation_of_L-Glutamine_Facilitated_by_Characterization_of_Non-Heme_Dioxygenases_from_Non-Ribosomal_Peptide_Biosyntheses/14206172

الاتاحة: https://doi.org/10.26434/chemrxiv.14206172.v1

المؤلفون: Mitra, Mainak, Brinkmeier, Alexander, Li, Yong, Borrell, Margarida, Call, Arnau, Fillol, Julio Lloret, Richmond, Michael G., Costas, Miquel, Nordlander, Ebbe

المصدر: Dalton Transactions, 52(12), Royal Society of Chemistry, January 5, 2023, pp. 1-14

مصطلحات موضوعية: steric influences, tautomers, stereospecific C-H hydroxylation

وصف الملف: 14 p.; Text

Relation: local-cont-no: d2dt00725h; https://digital.library.unt.edu/ark:/67531/metadc2179423/; ark: ark:/67531/metadc2179423

الاتاحة: https://doi.org/10.1039/D2DT00725H
https://digital.library.unt.edu/ark:/67531/metadc2179423/

المؤلفون: Runsheng Xu, Rongrong Cai, Sixian Zhou, Zhuoda Zhou, Beibei Li, Dihui Xu

المصدر: Molecules; Volume 22; Issue 11; Pages: 1912

مصطلحات موضوعية: reaction mechanism, Cu-catalyzed, C-H hydroxylation/C-S coupling, ESI-HR MS, DFT

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Computational and Theoretical Chemistry; https://dx.doi.org/10.3390/molecules22111912

الاتاحة: https://doi.org/10.3390/molecules22111912

المؤلفون: LIN YI

المساهمون: CHEMICAL & BIOMOLECULAR ENGINEERING, Zhi Li

مصطلحات موضوعية: C-H hydroxylation, P450pyr, directed evolution, FADS, microfluidics screening, high enantioselectiivity

Relation: LIN YI (2024-01-02). EVOLVING ENANTIOSELECTIVE P450 MONOOXYGENASE FOR BIOHYDROXYLATIONS WITH MICROFLUIDIC ENZYME SCREENING. ScholarBank@NUS Repository.; https://scholarbank.nus.edu.sg/handle/10635/247855; orcid:0000-0003-1273-9032

الاتاحة: https://scholarbank.nus.edu.sg/handle/10635/247855

المصدر: Organic Synthesis : State of the Art 2009 - 2011, 2013.

الاتاحة: https://doi.org/10.1093/oso/9780199965724.003.0043

المصدر: Organic Synthesis : State of the Art 2009 - 2011, 2013.

الاتاحة: https://doi.org/10.1093/oso/9780199965724.003.0019

المؤلفون: Kassin, Victor-Emmanuel H, Gerardy, Romaric, Toupy, Thomas, Collin, Diego, Salvadeo, Elena, Toussaint, Francois, Van Hecke, Kristof, Monbaliu, Jean-Christophe M

المصدر: GREEN CHEMISTRY ; ISSN: 1463-9262 ; ISSN: 1463-9270

مصطلحات موضوعية: Chemistry, AMINO KETONE REARRANGEMENTS, C-H HYDROXYLATION, CYCLIC-KETONES, THERMAL REARRANGEMENTS, OXYGEN, MECHANISM

وصف الملف: application/pdf

Relation: https://biblio.ugent.be/publication/8645681; http://hdl.handle.net/1854/LU-8645681; http://dx.doi.org/10.1039/c9gc00336c; https://biblio.ugent.be/publication/8645681/file/8645691

الاتاحة: https://biblio.ugent.be/publication/8645681
http://hdl.handle.net/1854/LU-8645681
https://doi.org/10.1039/c9gc00336c
https://biblio.ugent.be/publication/8645681/file/8645691

المؤلفون: Coleman, Tom, Wong, Siew Hoon, Podgorski, Matthew N., Bruning, John B., De Voss, James J., Bell, Stephen G.

مصطلحات موضوعية: P450-catalyzed N-dealkylation, C-H hydroxylation, Compound-I, Crystal-structure, Electron-transfer, Acid-derivatives, Oxidation, Epoxidation, Mechanism, System, 1503 Catalysis

Relation: orcid:0000-0002-2659-5140; DP140103229; FT140100355; Not set

الاتاحة: https://espace.library.uq.edu.au/view/UQ:240c1b3

المؤلفون: Gopalan Rajaraman, Azaj Ansari

المصدر: Phys. Chem. Chem. Phys.. 16:14601-14613

مصطلحات موضوعية: Axial Ligand, Iron, Molecular Conformation, General Physics and Astronomy, Hydroxylation, Ligands, Ring (chemistry), Photochemistry, Pi-Cation Radicals, Heterolysis, Stereospecific Alkane Hydroxylation, Catalysis, Amino Acids, Aromatic, chemistry.chemical_compound, Density-Functional Theory, Computational chemistry, Pyridine, Reactivity (chemistry), Ferrous Compounds, Physical and Theoretical Chemistry, Effective Core Potentials, Ligand, Ab-Initio, Hydrogen Peroxide, Spin Oxoiron(Iv) Complex, Homolysis, Oxygen, chemistry, Electrophile, Quantum Theory, C-H Hydroxylation, Iron-Catalyzed Oxidation, O Bond-Cleavage

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::758b339a0c7407ced2d5ebcc5df301de
https://doi.org/10.1039/c3cp55430a

المؤلفون: Abhishek Kaushik, Azaj Ansari, Gopalan Rajaraman

المصدر: Journal of the American Chemical Society. 135:4235-4249

مصطلحات موضوعية: Models, Molecular, Dioxygen Activation, Transition-Metal-Complexes, Oxidative phosphorylation, Hydroxylation, O-O Bond, Ferric Compounds, Electronic-Structure, Biochemistry, Catalysis, chemistry.chemical_compound, Colloid and Surface Chemistry, Density-Functional Theory, Computational chemistry, medicine, Organic chemistry, Effective Core Potentials, General Chemistry, Oxidants, Peroxides, chemistry, Mechanism (philosophy), Exchange-Enhanced Reactivity, Electrophile, Potential energy surface, Spin-State Energetics, Thermodynamics, Ferric, C-H Hydroxylation, Density functional theory, Alkane Hydroxylation, Dispersion (chemistry), Oxidation-Reduction, Iron Compounds, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be58c7816f259805b4ecb695fd2a4ea8
https://doi.org/10.1021/ja307077f

المؤلفون: Liang, Yu-Feng, Li, Xinyao, Wang, Xiaoyang, Zou, Miancheng, Tang, Conghui, Liang, Yujie, Song, Song, Jiao, Ning

المساهمون: Jiao, N (reprint author), Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Xue Yuan Rd 38, Beijing 100191, Peoples R China., Jiao, N (reprint author), Nankai Univ, State Key Lab Elementoorgan Chem, Weijin Rd 94, Tianjin 300071, Peoples R China., Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Xue Yuan Rd 38, Beijing 100191, Peoples R China., Nankai Univ, State Key Lab Elementoorgan Chem, Weijin Rd 94, Tianjin 300071, Peoples R China.

المصدر: EI ; PubMed ; SCI

مصطلحات موضوعية: C-H HYDROXYLATION, CATALYZED AEROBIC DEHYDROGENATION, DIMETHYL-SULFOXIDE, CARBONYL-COMPOUNDS, SUBSTITUTED CYCLOHEXANONES, OXIDATIVE AROMATIZATION, MOLECULAR-OXYGEN, HYDROBROMIC ACID, FACILE SYNTHESIS, SELECTIVE METHOD

Relation: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY.2016,138(37),12271-12277.; 1438823; http://hdl.handle.net/20.500.11897/493078; WOS:000384037400039

الاتاحة: https://hdl.handle.net/20.500.11897/493078
https://doi.org/10.1021/jacs.6b07269

المؤلفون: Liang, Yu-Feng, Wu, Kai, Song, Song, Li, Xinyao, Huang, Xiaoqiang, Jiao, Ning

المساهمون: Jiao, N (reprint author), Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Xue Yuan Rd 38, Beijing 100191, Peoples R China., Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China., Chinese Acad Sci, State Key Lab Organometall Chem, Shanghai 200062, Peoples R China., Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Xue Yuan Rd 38, Beijing 100191, Peoples R China.

المصدر: PubMed ; SCI

مصطلحات موضوعية: C-H HYDROXYLATION, ASYMMETRIC TRANSFER HYDROGENATION, ALKOXYSULFONIUM IONS, METHYL KETONES, FACILE ACCESS, OXIDATION, BONDS, FUNCTIONALIZATION, OXYGENATION, ALCOHOLS

Relation: ORGANIC LETTERS.2015,17,(4),876-879.; 650345; http://hdl.handle.net/20.500.11897/156269; WOS:000349942600029

الاتاحة: https://hdl.handle.net/20.500.11897/156269
https://doi.org/10.1021/ol5037387

المؤلفون: Lonsdale, Richard, Houghton, Kerensa T., Zurek, Jolanta, Bathelt, Christine M., Foloppe, Nicolas, de Groot, Marcel J., Harvey, Jeremy N., Mulholland, Adrian J.

المصدر: Lonsdale , R , Houghton , K T , Zurek , J , Bathelt , C M , Foloppe , N , de Groot , M J , Harvey , J N & Mulholland , A J 2013 , ' Quantum Mechanics/Molecular Mechanics Modeling of Regioselectivity of Drug Metabolism in Cytochrome P450 2C9 ' , Journal of the American Chemical Society , vol. 135 , no. 21 , pp. 8001-8015 . https://doi.org/10.1021/ja402016p

مصطلحات موضوعية: MOLECULAR-ORBITAL METHODS, C-H HYDROXYLATION, GAUSSIAN-BASIS SETS, ENZYME-CATALYZED REACTIONS, 2-STATE REBOUND MECHANISM, SUBSTRATE-BINDING SITE, AROMATIC HYDROXYLATION, COMPOUND-I, STEREOSELECTIVE METABOLISM, BENZENE HYDROXYLATION

الاتاحة: https://hdl.handle.net/1983/b91749e1-cde8-4a48-95a1-2e38c7bacf7e
https://research-information.bris.ac.uk/en/publications/b91749e1-cde8-4a48-95a1-2e38c7bacf7e
https://doi.org/10.1021/ja402016p

المؤلفون: JACCOB, M, RAJARAMAN, G

مصطلحات موضوعية: C-H Hydroxylation, Nonheme Oxoiron(Iv) Complexes, Hydrogen-Atom Abstraction, Effective Core Potentials, Parent Amido Complex, Axial Ligand, 2-State Reactivity, Cytochrome-P450 Enzymes, Aromatic Hydroxylation, Electronic-Structures

Relation: DALTON TRANSACTIONS, 41(34)10430-10439; http://dx.doi.org/10.1039/c2dt31071f; http://dspace.library.iitb.ac.in/jspui/handle/100/15589

الاتاحة: http://dspace.library.iitb.ac.in/jspui/handle/100/15589
https://doi.org/10.1039/c2dt31071f

المؤلفون: Gopalan Rajaraman, Madhavan Jaccob

المصدر: Dalton transactions (Cambridge, England : 2003). 41(34)

مصطلحات موضوعية: Cytochrome-P450 Enzymes, Nonheme Oxoiron(Iv) Complexes, Spin states, Axial Ligand, Chemistry, Nitrene, Hydrogen-Atom Abstraction, 2-State Reactivity, Parent Amido Complex, Electronic structure, Electronic-Structures, Inorganic Chemistry, Crystallography, Atomic orbital, Computational chemistry, C-H Hydroxylation, Molecular orbital, Reactivity (chemistry), Aromatic Hydroxylation, Ground state, Effective Core Potentials, Natural bond orbital

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9e445883657c228c90ccb85ee3651b2
https://pubmed.ncbi.nlm.nih.gov/22821241

المؤلفون: Schwartz, Brett D., Denton, Justin R., Bernhardt, Paul V., Davies, Huw M. L., Williams, Craig M.

المساهمون: D. Enders

مصطلحات موضوعية: hydroxyvibsanin E, C-H hydroxylation, Rubottom oxidation, C1, 970103 Expanding Knowledge in the Chemical Sciences, 0305 Organic Chemistry

Relation: orcid:0000-0001-6839-1763; orcid:0000-0002-3834-7398; R01 GM080337; R01 GM080337-04

الاتاحة: https://espace.library.uq.edu.au/view/UQ:197527

المؤلفون: Schwartz, Brett, Denton, Justin R, Bernhardt, Paul, Davies, Huw ML, Williams, Craig

المصدر: Synthesis

مصطلحات موضوعية: Keywords: C-H hydroxylation, Hydroxyvibsanin E, Rubottom oxidation, Stereo-selective, Total synthesis, Hydroxylation, Silanes, Oxidation, 15 o methylcyclovibsanin b, 3 hydroxyvibsanin e, 3 o methylfuranovibsanin a, furanovibsanin a, levo 5 epi vibsanin e, plant ext C-H hydroxylation

Relation: http://hdl.handle.net/1885/59633; https://openresearch-repository.anu.edu.au/bitstream/1885/59633/5/Towards_the_Total_Synthesis_of_3-Hydroxyvibsanin_E.pdf.jpg; https://openresearch-repository.anu.edu.au/bitstream/1885/59633/7/01_Schwartz_Towards_the_Total_Synthesis_of_2009.pdf.jpg

الاتاحة: http://hdl.handle.net/1885/59633
https://doi.org/10.1055/s-0029-1216912
https://openresearch-repository.anu.edu.au/bitstream/1885/59633/5/Towards_the_Total_Synthesis_of_3-Hydroxyvibsanin_E.pdf.jpg
https://openresearch-repository.anu.edu.au/bitstream/1885/59633/7/01_Schwartz_Towards_the_Total_Synthesis_of_2009.pdf.jpg