المؤلفون: Yin, Xiang

المساهمون: University/Department: Universitat Rovira i Virgili. Departament de Química Analítica i Química Orgànica

Thesis Advisors: Echavarren Pablos, Antonio Maria

المصدر: TDX (Tesis Doctorals en Xarxa)

مصطلحات موضوعية: cicloheptatriens, reacció retro-Buchner, carbens d'or (I), cicloheptatrienos, reacción retro-Buchner, carbenos de oro (I), cycloheptatrienes, retro-Buchner reaction, gold(I) carbene, Ciències

وصف الملف: application/pdf

URL الوصول: http://hdl.handle.net/10803/665105

المؤلفون: Herlé, Bart

المساهمون: University/Department: Universitat Rovira i Virgili. Departament de Química Analítica i Química Orgànica

Thesis Advisors: Echavarren Pablos, Antonio M.

المصدر: TDX (Tesis Doctorals en Xarxa)

مصطلحات موضوعية: carbens d’or(I), ciclopropanació, reacció de retro-Buchner, carbenos de oro(I), ciclopropanación, reacción de retro-Buchner, gold(I) carbenes, cyclopropanation, retro-Buchner reaction, Ciències

وصف الملف: application/pdf

URL الوصول: http://hdl.handle.net/10803/454770

المؤلفون: Tuyen Phung, Bich, Medini, Amira, Maldivi, Pascale, Poisson, Jean‐françois, Bessières, Bernard, Darses, Benjamin

المساهمون: Département de Chimie Moléculaire - Synthèse Et Réactivité en Chimie Organique (DCM - SeRCO), Département de Chimie Moléculaire (DCM), Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes (UGA)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes (UGA), SYstèmes Moléculaires et nanoMatériaux pour l’Energie et la Santé (SYMMES), Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche Interdisciplinaire de Grenoble (IRIG), Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Grenoble Alpes (UGA)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP), Université Grenoble Alpes (UGA), Conception d’Architectures Moléculaires et Processus Electroniques (CAMPE), Université Grenoble Alpes (UGA)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche Interdisciplinaire de Grenoble (IRIG), ANR-17-EURE-0003,CBH-EUR-GS,CBH-EUR-GS(2017)

المصدر: ISSN: 1615-4150.

مصطلحات موضوعية: carbene, rhodium, DFT calculations, Buchner reaction, aromatic cyclopropanation, C-H insertion, [CHIM.ORGA]Chemical Sciences/Organic chemistry

الاتاحة: https://hal.science/hal-04682171
https://hal.science/hal-04682171v1/document
https://hal.science/hal-04682171v1/file/Manuscript_HAL.pdf
https://doi.org/10.1002/adsc.202400527

المؤلفون: Zheng, Yongkun

Thesis Advisors: Leyva Perez, Antonio, Mon Conejero, Marta, Universitat Politècnica de València. Instituto Universitario Mixto de Tecnología Química - Institut Universitari Mixt de Tecnologia Química

مصطلحات موضوعية: Carbenos, Plata, Zeolitas, Catálisis, Reacción de Buchner, Reacción de inserción C-H, C-H insertion reaction, Buchner reaction, Catalysis, Zeolites, Silver, Carbenes, 09.- Desarrollar infraestructuras resilientes, promover la industrialización inclusiva y sostenible, y fomentar la innovación

الاتاحة: http://hdl.handle.net/10251/207244

المؤلفون: Ji, Kegong, Zhang, Liming

المصدر: Advanced Synthesis & Catalysis. 360(4)

مصطلحات موضوعية: Inorganic Chemistry, Organic Chemistry, Chemical Sciences, Cyclopropanation, Gold Carbene, Oxidation, Buchner reaction, Cycloheptatriene, Chemical Engineering, Organic chemistry

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/2jb0m654
https://escholarship.org/content/qt2jb0m654/qt2jb0m654.pdf

المؤلفون: Rodríguez Márquez, Irene, Villalobos Romero, Federico, Cuerva Carvajal, Juan Manuel, González Campaña, Araceli

مصطلحات موضوعية: On-surface synthesis, Graphene nanoribbons, Retro-Buchner reaction, Intramolecular rearrangement, Scanning tunneling microscope, Non-contact atomic force microscope, CO functionalized tip, X-ray photoelectron spectroscopy

Relation: info:eu-repo/grantAgreement/EC/H2020/696656; info:eu-repo/grantAgreement/EC/H2020/785219; info:eu-repo/grantAgreement/ERC/H2020/2013-SYG-610256 NANOCOSMOS; info:eu-repo/grantAgreement/ERC/H2020/2015-STG-677023; info:eu-repo/grantAgreement/EC/H2020/MAT2017-85089-C2-1-R; info:eu-repo/grantAgreement/EC/H2020/PGC2018-101181-B-I00; Márquez, I.R.; Ruíz del Árbol, N.; Urgel, J.I.; Villalobos, F.; Fasel, R.; López, M.F.; Cuerva, J.M.; Martín-Gago, J.A.; Campaña, A.G.; Sánchez-Sánchez, C. On-Surface Thermal Stability of a Graphenic Structure Incorporating a Tropone Moiety. Nanomaterials 2022, 12, 488. [https://doi.org/10.3390/nano12030488]; http://hdl.handle.net/10481/72809

الاتاحة: http://hdl.handle.net/10481/72809
https://doi.org/10.3390/nano12030488

المؤلفون: Buckley, Aoife, Crowley, Daniel C., Brouder, Thomas A., Ford, Alan, Khandavilli, Udaya Bhaskara Rao, Lawrence, Simon E., Maguire, Anita R.

مصطلحات موضوعية: Intramolecular buchner reaction, Sigmatropic rearrangement, Asymmetric-synthesis, Carbene insertion, HIV-1 integrase, Complexes, Bond, Functionalization, Diazoketones, Derivatives

وصف الملف: application/pdf

Relation: info:eu-repo/grantAgreement/SFI/SFI Research Centres/12/RC/2275/IE/Synthesis and Solid State Pharmaceutical Centre (SSPC)/; Buckley, A. M., Crowley D. C., Brouder; T. A., Ford, A; Khandavilli, U. B. R., Lawrence, S. E. and Maguire, A. R. (2021) 'Dirhodium carboxylate catalysts from 2-fenchyloxy or 2-menthyloxy arylacetic acids: enantioselective C-H insertion, aromatic addition and oxonium ylide formation/rearrangement', ChemCatChem, 13 , pp. 4318-4324. doi:10.1002/cctc.202100924; 4324; ChemCatChem; 4318; https://hdl.handle.net/10468/12603; 13

الاتاحة: https://hdl.handle.net/10468/12603
https://doi.org/10.1002/cctc.202100924

المؤلفون: Ekaterina E. Galenko (3093012), Vladimir A. Bodunov (4326568), Mariya A. Kryukova (8479695), Mikhail S. Novikov (1537957), Alexander F. Khlebnikov (1537960)

مصطلحات موضوعية: Biophysics, Biochemistry, Sociology, Chemical Sciences not elsewhere classified, Buchner reaction, cycloheptatriene-norcaradiene valen., valence isomers, azirine fragment, norcaradiene isomers, cycloheptatriene form, Cycloheptatriene valence isomer, Cycloheptatriene Containing Nitroge., chloroform solution, pyrrole, X-ray analysis, NMR, reaction conditions, 4 catalysis, Reductive isoxazole ring opening, DFT calculations, cycloheptatriene isomers, equilibrium mixture, TFA, room temperature

Relation: https://figshare.com/articles/journal_contribution/Buchner_Reaction_Azirine_Modification_Approach_Toward_Cycloheptatriene_Containing_Nitrogen_Heterocyclic_Scaffolds/13931524

الاتاحة: https://doi.org/10.1021/acs.joc.0c02928.s001

المؤلفون: Phung, Bich Tuyen

المساهمون: Département de Chimie Moléculaire (DCM), Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes (UGA), Université Grenoble Alpes 2020-., Bernard Bessières, Benjamin Darses

المصدر: https://theses.hal.science/tel-04651531 ; Autre. Université Grenoble Alpes [2020-.], 2024. Français. ⟨NNT : 2024GRALV004⟩.

مصطلحات موضوعية: Selectivity, Buchner reaction, Asymmetric catalysis, Organic Synthessis, Réaction de Buchner, Catalyse asymétrique, Sélectivité, Synthèse organique, [CHIM.OTHE]Chemical Sciences/Other

Relation: NNT: 2024GRALV004

الاتاحة: https://theses.hal.science/tel-04651531
https://theses.hal.science/tel-04651531v1/document
https://theses.hal.science/tel-04651531v1/file/PHUNG_2024_archivage.pdf

المؤلفون: Jun-ichi Matsuo, Shunya Morita, Tomoyuki Yoshimura

المصدر: Chemical and Pharmaceutical Bulletin. 2019, 67(7):729

المؤلفون: Herle, Bart, Holstein, Philipp M., Echavarren, Antonio M.

المساهمون: Química Analítica i Química Orgànica, Universitat Rovira i Virgili

المصدر: Acs Catalysis ; https://pubs.acs.org/doi/10.1021/acscatal.7b00737 ; 10.1021/acscatal.7b00737 ; Acs Catalysis. 7 (5): 3668-3675

مصطلحات موضوعية: Catalysis,Chemistry (Miscellaneous),Chemistry, Physical, cycloheptatrienes, cyclopropanation, gold catalysis, retro-buchner reaction, Vinylcyclopropanes, Astronomia / física, Catalysis, Chemistry (miscellaneous), Chemistry, Ciências agrárias i, Engenharias ii, General chemistry, Interdisciplinar, Materiais, Química

Relation: http://hdl.handle.net/20.500.11797/imarina3654606

الاتاحة: https://hdl.handle.net/20.500.11797/imarina3654606

المؤلفون: Sung Hwan Park, Shou-Guo Wang, Nicolai Cramer

المصدر: ACS Catalysis. 9:10226-10231

مصطلحات موضوعية: cyclization, cp ligands, rearrangement, chemistry.chemical_element, reduction, 010402 general chemistry, 01 natural sciences, isomerization, Catalysis, insertion, Cyclopropane, chemistry.chemical_compound, chiral cyclopentadienyl ligands, ruthenium, buchner reaction, complexes, 010405 organic chemistry, Chemistry, Enantioselective synthesis, asymmetric catalysis, General Chemistry, Combinatorial chemistry, 0104 chemical sciences, Ruthenium, Coupling (electronics), cyclopropane, Isomerization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a527f6ef91d43b8fc476cf744b3339f4
https://doi.org/10.1021/acscatal.9b03858

المؤلفون: Kazutake Hagiya, Masami Kagawa, Naoko Ohuchi, Tadashi Okuyama, Takashi Sugimura, 大内 直子, 奥山 格, 杉村 高志, 萩谷 一剛, 香川 昌巳

المصدر: Abstracts of Symposium on Physical Organic Chemistry. 2003, :83

المؤلفون: Antonio M. Echavarren, Bart Herlé, Philipp M. Holstein

المصدر: RECERCAT (Dipòsit de la Recerca de Catalunya)
ACS Catalysis
Recercat. Dipósit de la Recerca de Catalunya
instname

مصطلحات موضوعية: Allylic rearrangement, 010405 organic chemistry, Cyclopropanation, Chemistry, Cycloheptatriene, cyclopropanation, vinylcyclopropanes, General Chemistry, 010402 general chemistry, 01 natural sciences, Combinatorial chemistry, Catalysis, gold catalysis, 0104 chemical sciences, chemistry.chemical_compound, retro-Buchner reaction, cycloheptatrienes, Reagent, Organic chemistry, Stereoselectivity, Selectivity, Isomerization, Research Article

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe398fd48cc056d164f2080d2b0f1b5b
https://hdl.handle.net/2072/335514

المؤلفون: Cristina García-Morales, Mihai Raducan, Antonio M. Echavarren, Ekaterina S. Smirnova, Juan Manuel Sarria Toro

المصدر: RECERCAT (Dipòsit de la Recerca de Catalunya)
Recercat. Dipósit de la Recerca de Catalunya
instname
Angewandte Chemie (International Ed. in English)
Angewandte Chemie International Edition

مصطلحات موضوعية: Cyclopropanation, cyclopropanation, 010402 general chemistry, Chloride, 01 natural sciences, Catalysis, chemistry.chemical_compound, Polymer chemistry, medicine, Organic chemistry, Reactivity (chemistry), Olefin fiber, 010405 organic chemistry, Communication, General Chemistry, General Medicine, gold, Communications, 3. Good health, 0104 chemical sciences, Carbenoids, carbenes, Buchner ring expansion, chemistry, Buchner reaction, Trimethylsilyldiazomethane, Carbene, Phosphine, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b5e92900e2823a3009e23ab0bc3b8d3
http://hdl.handle.net/2072/334737

المؤلفون: Zhang, Zhikun, Feng, Jiajie, Xu, Yan, Zhang, Songnan, Ye, Yuxuan, Li, Tianjiao, Wang, Xi, Chen, Jun, Zhang, Yan, Wang, Jianbo

المساهمون: Wang, X (reprint author), Peking Univ, BNLMS, Beijing 100871, Peoples R China., Peking Univ, BNLMS, Beijing 100871, Peoples R China., Peking Univ, Key Lab Bioorgan Chem & Mol Engn, Minist Educ, Coll Chem, Beijing 100871, Peoples R China., Beijing Inst Microchem, Beijing 100091, Peoples R China.

المصدر: SCI

مصطلحات موضوعية: diazo compounds, carbene, trifluoromethylation, Buchner reaction, cycloheptatriene, ALPHA-DIAZOCARBONYL COMPOUNDS, ENANTIOSELECTIVE TRIFLUOROMETHYLATION, CATALYZED TRIFLUOROMETHYLATION, PERFLUOROALKYLATION REACTIONS, ASYMMETRIC FLUORINATION, FUNCTIONAL-GROUPS, REAGENTS, TRANSFORMATIONS, STRATEGIES, INSERTION

Relation: SYNLETT.2015,26,(1),59-62.; 752992; http://hdl.handle.net/20.500.11897/387235; WOS:000346492100009

الاتاحة: https://hdl.handle.net/20.500.11897/387235
https://doi.org/10.1055/s-0034-1378937

المؤلفون: Liu, Zhenxing, Tan, Haocheng, Wang, Long, Fu, Tianren, Xia, Ying, Zhang, Yan, Wang, Jianbo

المساهمون: Wang, JB (reprint author), Peking Univ, Coll Chem, Minist Educ, Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China., Peking Univ, Coll Chem, Minist Educ, Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China., Peking Univ, Coll Chem, Minist Educ, Key Lab Bioorgan Chem & Mol Engn, Beijing 100871, Peoples R China., Chinese Acad Sci, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China.

المصدر: PubMed ; SCI

مصطلحات موضوعية: aromatic substitution, Buchner reaction, carbenes, diazo compounds, fluorenes, C-H INSERTION, ALPHA-DIAZOCARBONYL COMPOUNDS, BOND FUNCTIONALIZATION, RHODIUM(II) ACETATE, CARBONYL-COMPOUNDS, COUPLING REACTIONS, BORONIC ACIDS, DIAZO GROUP, TOSYLHYDRAZONES

Relation: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION.2015,54,(10),3056-3060.; 650512; http://hdl.handle.net/20.500.11897/188410; WOS:000350302300032

الاتاحة: https://hdl.handle.net/20.500.11897/188410
https://doi.org/10.1002/anie.201409982

المؤلفون: Ring, Aoife

المساهمون: Maguire, Anita R.

مصطلحات موضوعية: C-H insertion, Copper catalysis, Diazocarbonyl, Lactams, Sulfones, Buchner reaction, Rhodium catalysis, Enantioselective, Bisoxazoline

وصف الملف: application/pdf

Relation: Ring, A. 2016. Enantioselective transformations of α-diazocarbonyl compounds; catalyst and substrate effects. PhD Thesis, University College Cork.; 451; http://hdl.handle.net/10468/4036

الاتاحة: http://hdl.handle.net/10468/4036

المؤلفون: Leslie-Ann Clarke, Aoife Ring, Alan Ford, Anita R. Maguire, Catherine N. Slattery, Shane T. O'Neill

المصدر: Synlett. 23:765-767

مصطلحات موضوعية: Addition reaction, Bonds, Chemistry, Organic Chemistry, Diazocarbonyl, Enantioselective synthesis, chemistry.chemical_element, Copper, Copper catalysis, Complexes, Research council, Bis(oxazoline) ligands, Organic chemistry, Buchner reaction, C-H insertion, Carbene insertion

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ab5fc98d05a751716d8adbee74198e0
https://doi.org/10.1055/s-0031-1290598

المؤلفون: Nani, Roger Rauhauser

مصطلحات موضوعية: natural product synthesis, Chemistry, diazo compounds, salvileucalin B, cyclopropanation, Buchner reaction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::f60a53397ff1fd82b7ce4b0b71c77e5d