يعرض 1 - 10 نتائج من 10 نتيجة بحث عن '"O. Stephen Ojo"', وقت الاستعلام: 1.03s تنقيح النتائج
  1. 1
    An expedient copper-catalysed asymmetric synthesis of γ-lactones and γ-lactams. Application to the synthesis of lucidulactone A

    المؤلفون: O. Stephen Ojo, David L. Hughes, Christopher J. Richards

    المصدر: Organic & Biomolecular Chemistry. 21:4144-4149

    مصطلحات موضوعية: Organic Chemistry, Physical and Theoretical Chemistry, Biochemistry

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0ee5eef64dbf2b81d74a713a96cab2cc
    https://doi.org/10.1039/d3ob00563a

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  2. 2
    دورية أكاديمية

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  3. 3
    Bacterial catabolism of β-hydroxypropiovanillone and β-hydroxypropiosyringone produced in the reductive cleavage of arylglycerol-β-aryl ether in lignin

    المؤلفون: Yudai Higuchi, Christopher S. Lancefield, Hiroki Takenami, Nicholas J. Westwood, Naofumi Kamimura, O. Stephen Ojo, Shogo Aoki, Shojiro Hishiyama, Yoshihiro Katayama, Eiji Masai, Kenji Takahashi

    المساهمون: University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM, University of St Andrews. Biomedical Sciences Research Complex

    مصطلحات موضوعية: 0301 basic medicine, 030106 microbiology, NDAS, Aldehyde dehydrogenase, Ether, Applied Microbiology and Biotechnology, Lignin, Cofactor, 03 medical and health sciences, chemistry.chemical_compound, Oxidoreductase, Escherichia coli, Glucose-methanol-choline oxidoreductase, QD, Ether cleavage, Enzyme Gene, chemistry.chemical_classification, Ecology, biology, Catabolism, Lyase, QD Chemistry, Sphingobium, Sphingomonadaceae, chemistry, Biochemistry, Genes, Bacterial, biology.protein, Biodegradation, b-aryl ether, Microorganisms, Genetically-Modified, Food Science, Biotechnology, Ethers

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::048f7839c708d18b3f81cf51f1a3031c
    https://hdl.handle.net/10023/15709

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  4. 4
    Synthesis of the natural product descurainolide and cyclic peptides from lignin-derived aromatics

    المؤلفون: Brunello Nardone, James E. Taylor, Andrew R. Neal, Alexandra M. Z. Slawin, O. Stephen Ojo, Tomas Lebl, Liam Wilson, Stefania Francesca Musolino, James H. Naismith, Andrew D. Smith, Nicholas J. Westwood, David B. Cordes

    المساهمون: EPSRC, The Leverhulme Trust, University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM, University of St Andrews. Biomedical Sciences Research Complex

    المصدر: Organic & Biomolecular Chemistry. 16(2)

    مصطلحات موضوعية: Allylic rearrangement, Macrocyclic Compounds, 010402 general chemistry, 01 natural sciences, Biochemistry, Lignin, Peptides, Cyclic, Kinetic resolution, chemistry.chemical_compound, Lactones, Organic chemistry, QD, Physical and Theoretical Chemistry, chemistry.chemical_classification, Substitution reaction, Biological Products, Natural product, 010405 organic chemistry, Vanillin, Organic Chemistry, food and beverages, DAS, Stereoisomerism, QD Chemistry, Cyclic peptide, 0104 chemical sciences, Amino acid, chemistry, Cyclization, Benzaldehydes, Tyrosine

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26a97e4a791c891f36a078709e840747
    http://ora.ox.ac.uk/objects/uuid:

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  5. 5
    Isolation of Functionalized Phenolic Monomers through Selective Oxidation and CO Bond Cleavage of the β‐O‐4 Linkages in Lignin

    المؤلفون: Nicholas J. Westwood, Christopher S. Lancefield, O. Stephen Ojo, Fanny Tran

    المصدر: Angewandte Chemie International Edition. 54:258-262

    مصطلحات موضوعية: Depolymerization, fungi, Organosolv, food and beverages, chemistry.chemical_element, General Medicine, General Chemistry, Zinc, Oxidants, Highly selective, Lignin, Catalysis, Polymerization, chemistry.chemical_compound, Monomer, Phenols, chemistry, Catalytic oxidation, Benzoquinones, Organic chemistry, Oxidation-Reduction, Bond cleavage

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ea6a1bfb9807569bd19f610f81c2efb
    https://doi.org/10.1002/anie.201409408

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  6. 6
    A convenient, economical and scalable multi-gram synthesis of 1-vinylcyclopropyl 4-methylbenzenesulfonate

    المؤلفون: O. Stephen Ojo, Phillip A. Inglesby, P. Andrew Evans, Daniela E. Negru

    المصدر: Org. Chem. Front.. 1:821-824

    مصطلحات موضوعية: chemistry.chemical_classification, Alicyclic compound, Cycloisomerization, chemistry, Organic Chemistry, Scalability, Combinatorial chemistry, Gram

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::8497ff824fed53c62b6cd1121070de77
    https://doi.org/10.1039/c4qo00089g

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  7. 7
    The synthesis and analysis of lignin-bound Hibbert ketone structures in technical lignins

    المؤلفون: Calum Hand, Tomas Lebl, Isabella Panovic, Andrew R. Neal, James R. D. Montgomery, O. Stephen Ojo, Christopher S. Lancefield, Daniel M. Miles-Barrett, Nicholas J. Westwood, David B. Cordes, Alexandra M. Z. Slawin

    المساهمون: EPSRC, University of St Andrews. School of Chemistry, University of St Andrews. EaSTCHEM, University of St Andrews. Biomedical Sciences Research Complex

    المصدر: Miles-Barrett, D M, Neal, A R, Hand, C, Montgomery, J R D, Panovic, I, Ojo, O S, Lancefield, C S, Cordes, D B, Slawin, A M Z, Lebl, T & Westwood, N J 2016, ' The synthesis and analysis of lignin-bound Hibbert ketone structures in technical lignins ', Org. Biomol. Chem. . https://doi.org/10.1039/c6ob01915c

    مصطلحات موضوعية: Ketone, Organosolv, Lignocellulosic biomass, Chemistry Techniques, Synthetic, 010402 general chemistry, Lignin, 01 natural sciences, Biochemistry, chemistry.chemical_compound, Organic chemistry, Reactivity (chemistry), QD, Physical and Theoretical Chemistry, Douglas fir, chemistry.chemical_classification, Aqueous solution, 010405 organic chemistry, Organic Chemistry, DAS, Hydrogen-Ion Concentration, Ketones, QD Chemistry, Wood, 0104 chemical sciences, chemistry, Heteronuclear single quantum coherence spectroscopy

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b69f6090f3a5f147d7b03bcc6b83a37
    http://www.rsc.org/suppdata/c6/ob/c6ob01915c/c6ob01915c1.pdf

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  8. 8
    Isothiourea-Catalysed Acylative Kinetic Resolution of Aryl-Alkenyl (sp

    المؤلفون: Stefania F, Musolino, O Stephen, Ojo, Nicholas J, Westwood, James E, Taylor, Andrew D, Smith

    المصدر: Chemistry (Weinheim an Der Bergstrasse, Germany)

    مصطلحات موضوعية: isothiourea, Full Paper, Organocatalysis, acylation, kinetic resolution, Full Papers, renewable resources

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::82b6fc9d6185051879042d2c006d5789
    https://pubmed.ncbi.nlm.nih.gov/27775200

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  9. 9
    دورية أكاديمية

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    View record in Scopus
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  10. 10
    Retraction: Synthesis of a chiral dinuclear Cu(II)-benzothiazolamine complex: evidence of cuprophilic interaction in its structure and exploration of its electrochemical properties and catalytic performance.

    المؤلفون: Stephen Ojo O; WestCHEM, School of Chemistry, The Joseph Black Building, University of Glasgow, Glasgow, G12 8QQ, UK. Oluwarotimi.ojo@glasgow.ac.uk., Sale H; WestCHEM, School of Chemistry, The Joseph Black Building, University of Glasgow, Glasgow, G12 8QQ, UK. Oluwarotimi.ojo@glasgow.ac.uk., Symes MD; WestCHEM, School of Chemistry, The Joseph Black Building, University of Glasgow, Glasgow, G12 8QQ, UK. Oluwarotimi.ojo@glasgow.ac.uk., Wilson C; WestCHEM, School of Chemistry, The Joseph Black Building, University of Glasgow, Glasgow, G12 8QQ, UK. Oluwarotimi.ojo@glasgow.ac.uk.

    المصدر: Dalton transactions (Cambridge, England : 2003) [Dalton Trans] 2024 Feb 27; Vol. 53 (9), pp. 4343. Date of Electronic Publication: 2024 Feb 27.

    نوع المنشور: Retraction of Publication

    بيانات الدورية: Publisher: Royal Society of Chemistry Country of Publication: England NLM ID: 101176026 Publication Model: Electronic Cited Medium: Internet ISSN: 1477-9234 (Electronic) Linking ISSN: 14779226 NLM ISO Abbreviation: Dalton Trans Subsets: PubMed not MEDLINE; MEDLINE

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