المؤلفون: Nigro, Giuliano, Bourcier, Sophie, Lazennec-Schurdevin, Christine, Schmitt, Emmanuelle, Marlière, Philippe, Mechulam, Yves

المساهمون: Laboratoire de Biochimie de l'Ecole polytechnique (BIOC), École polytechnique (X), Institut Polytechnique de Paris (IP Paris)-Institut Polytechnique de Paris (IP Paris)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Chimie Moléculaire (LCM), Génomique métabolique (UMR 8030), Genoscope - Centre national de séquençage Evry (GENOSCOPE), Université Paris-Saclay-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 Paris-Saclay-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 d'Évry-Val-d'Essonne (UEVE)-Centre National de la Recherche Scientifique (CNRS)

المصدر: ISSN: 1047-8477.

مصطلحات موضوعية: Beta amino acid, Non-standard amino acid, Translation, X-ray crystallography, tRNA aminoacylation, [SDV.BBM.BS]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Structural Biology [q-bio.BM]

Relation: info:eu-repo/semantics/altIdentifier/pmid/31862305; PUBMED: 31862305

الاتاحة: https://polytechnique.hal.science/hal-02493753
https://polytechnique.hal.science/hal-02493753v1/document
https://polytechnique.hal.science/hal-02493753v1/file/1-s2.0-S1047847719302643-main.pdf
https://doi.org/10.1016/j.jsb.2019.107435

المؤلفون: S. Panzeri, D. Arosio, S. Gazzola, L. Belvisi, M. Civera, D. Potenza, F. Vasile, I. Kemker, T. Ertl, N. Sewald, O. Reiser, U. Piarulli

المساهمون: S. Panzeri, D. Arosio, S. Gazzola, L. Belvisi, M. Civera, D. Potenza, F. Vasile, I. Kemker, T. Ertl, N. Sewald, O. Reiser, U. Piarulli

مصطلحات موضوعية: peptidomimetic, integrin ligand, beta-amino acid, NMR conformational analysis, Settore CHIM/06 - Chimica Organica

Relation: info:eu-repo/semantics/altIdentifier/pmid/33339382; info:eu-repo/semantics/altIdentifier/wos/WOS:000603191300001; volume:25; issue:24; firstpage:1; lastpage:15; numberofpages:15; journal:MOLECULES; http://hdl.handle.net/2434/799879; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85098745666

الاتاحة: http://hdl.handle.net/2434/799879
https://doi.org/10.3390/molecules25245966

المؤلفون: Dao Thi, Hang, Van Nguyen, Tuyen, D'hooghe, Matthias

المصدر: MONATSHEFTE FUR CHEMIE ; ISSN: 0026-9247 ; ISSN: 1434-4475

مصطلحات موضوعية: Chemistry, Heterocycles, Strained molecules, Fluorine chemistry, Cyclizations, Ring opening, BETA-AMINO-ACID, BUILDING-BLOCKS, STAUDINGER REACTION, STEREOSELECTIVE-SYNTHESIS, TRIFLUOROMETHYL IMINE, MEDICINAL CHEMISTRY, AZIRIDINES, AZETIDINES, LACTAMS, KETONES

وصف الملف: application/pdf

Relation: https://biblio.ugent.be/publication/8544832; http://hdl.handle.net/1854/LU-8544832; http://dx.doi.org/10.1007/s00706-017-2134-2; https://biblio.ugent.be/publication/8544832/file/8544833

الاتاحة: https://biblio.ugent.be/publication/8544832
http://hdl.handle.net/1854/LU-8544832
https://doi.org/10.1007/s00706-017-2134-2
https://biblio.ugent.be/publication/8544832/file/8544833

المؤلفون: M.L. Gelmi, A. Contini, A. Bonetti, R. Bucci, D. Tessaro, F. Clerici, S. Pellegrino, D. Nava

المساهمون: M.L. Gelmi, A. Contini, A. Bonetti, R. Bucci, D. Tessaro, F. Clerici, S. Pellegrino, D. Nava

مصطلحات موضوعية: tetrahydroisoquinoline-4-carboxylic acid, beta-amino acid, enzymatic resolution, peptide, turn inducer, Settore CHIM/06 - Chimica Organica

Relation: info:eu-repo/semantics/altIdentifier/pmid/28467649; info:eu-repo/semantics/altIdentifier/wos/WOS:000407397300018; volume:23; issue:45; firstpage:10822; lastpage:10831; numberofpages:10; journal:CHEMISTRY-A EUROPEAN JOURNAL; http://hdl.handle.net/2434/494894; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85024402334

الاتاحة: http://hdl.handle.net/2434/494894
https://doi.org/10.1002/chem.201701045

المؤلفون: Engel, U., Syldatk, C., Rudat, J.

المصدر: AMB express, 2 (1), 33 ; ISSN: 2191-0855

مصطلحات موضوعية: Beta-amino acid, Dihydropyrimidinase, Hydantoinase, Carbamoylase, ddc:660, Chemical engineering, info:eu-repo/classification/ddc/660

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/wos/000209443000033; info:eu-repo/semantics/altIdentifier/issn/2191-0855; https://publikationen.bibliothek.kit.edu/1000033254; https://publikationen.bibliothek.kit.edu/1000033254/8303924; https://doi.org/10.5445/IR/1000033254; http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:swb:90-332549

الاتاحة: https://publikationen.bibliothek.kit.edu/1000033254
https://publikationen.bibliothek.kit.edu/1000033254/8303924
https://doi.org/10.5445/IR/1000033254
http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:swb:90-332549

المؤلفون: Palkó, Márta, Hänninen, Mikko M., Sillanpää, Reijo, Fülöp, Ferenc

مصطلحات موضوعية: bicyclic beta-amino acid derivatives, constrained chiral beta-amino acids, resolution, continuous flow hydrogenations

وصف الملف: 15080-15093; application/pdf

Relation: Molecules; http://www.mdpi.com/1420-3049/18/12/15080; 12; 18; CONVID_23768509

الاتاحة: http://urn.fi/URN:NBN:fi:jyu-201408282674

المؤلفون: Emmanuelle Schmitt, Sophie Bourcier, Christine Lazennec-Schurdevin, Giuliano Nigro, Yves Mechulam, Philippe Marliere

المساهمون: Laboratoire de Biochimie de l'Ecole polytechnique (BIOC), École polytechnique (X)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de chimie moléculaire (LCM), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-École polytechnique (X), Génomique métabolique (UMR 8030), Genoscope - Centre national de séquençage [Evry] (GENOSCOPE), Université Paris-Saclay-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 Paris-Saclay-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)-Centre National de la Recherche Scientifique (CNRS)-Université d'Évry-Val-d'Essonne (UEVE), École polytechnique (X)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université d'Évry-Val-d'Essonne (UEVE)-Centre National de la Recherche Scientifique (CNRS)

المصدر: Journal of Structural Biology
Journal of Structural Biology, Elsevier, 2020, 209 (2), pp.107435. ⟨10.1016/j.jsb.2019.107435⟩
Journal of Structural Biology, 2020, 209 (2), pp.107435. ⟨10.1016/j.jsb.2019.107435⟩

مصطلحات موضوعية: chemistry.chemical_classification, 0303 health sciences, Translation, Methionine, [SDV.BBM.BS]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Structural Biology [q-bio.BM], 030302 biochemistry & molecular biology, Beta amino acid, tRNA aminoacylation, Translation (biology), Aminoacylation, medicine.disease_cause, Amino acid, 03 medical and health sciences, chemistry.chemical_compound, Enzyme, Biochemistry, chemistry, Structural Biology, Transfer RNA, medicine, TRNA aminoacylation, Escherichia coli, 030304 developmental biology, Non-standard amino acid, X-ray crystallography

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4278facce4de3da795db20ae6d71d2f8
https://hal-polytechnique.archives-ouvertes.fr/hal-02493753/document

المؤلفون: Asuka Sato, Norio Sakai, Takeo Konakahara, 佐藤 あすか, 坂井 教郎, 小中原 猛雄

المصدر: Proceedings of the Symposium on Progress in Organic Reactions and Syntheses. 2008, :27

المؤلفون: Hiroshi Shiraki, Kazuhiko Takahashi, Kazuyoshi Takeda, Yoshitomo Suhara, 武田 収功, 白木 洋, 須原 義智, 高橋 和彦

المصدر: Proceedings of the Symposium on Progress in Organic Reactions and Syntheses. 2010, :48

المؤلفون: Kentaro Yamaguchi, Masahiro Hosoya, Masatoshi Kawahata, Tomohiko Ohwada, Yuko Otani, 大和田 智彦, 尾谷 優子, 山口 健太郎, 川幡 正俊, 細谷 昌弘

المصدر: Proceedings of the Symposium on Progress in Organic Reactions and Syntheses. 2011, :102

المؤلفون: Kentaro Yamaguchi, Masahiro Hosoya, Masatoshi Kawahata, Tomohiko Ohwada, Yuko Otani, 大和田 智彦, 尾谷 優子, 山口 健太郎, 川幡 正俊, 細谷 昌弘

المصدر: Abstracts of Symposium on Physical Organic Chemistry. 2011, :36

المؤلفون: Kentaro Yamaguchi, Masatoshi Kawahata, Tetsuharu Hori, Tomohiko Ohwada, Yuko Otani, 堀 徹治, 大和田 智彦, 尾谷 優子, 山口 健太郎, 川幡 正俊

المصدر: Abstracts of Symposium on Physical Organic Chemistry. 2008, :350

المؤلفون: Hang Dao Thi, Matthias D'hooghe, Tuyen Van Nguyen

المصدر: MONATSHEFTE FUR CHEMIE

مصطلحات موضوعية: AZETIDINES, Heterocycles, Cyclizations, 010402 general chemistry, STAUDINGER REACTION, 01 natural sciences, AZIRIDINES, chemistry.chemical_compound, Biological property, KETONES, Molecule, Reactivity (chemistry), Staudinger reaction, MEDICINAL CHEMISTRY, TRIFLUOROMETHYL IMINE, Trifluoromethyl, Fluorine chemistry, 010405 organic chemistry, Synthon, Ring opening, General Chemistry, Strained molecules, Combinatorial chemistry, 0104 chemical sciences, Chemistry, STEREOSELECTIVE-SYNTHESIS, chemistry, BETA-AMINO-ACID, LACTAMS, BUILDING-BLOCKS

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a413ab8b4f550c20de5e333da1fbaca8
https://biblio.ugent.be/publication/8544832/file/8544833

المؤلفون: Samantha Deianira Dattoli, Santi Spampinato, Arianna Greco, Monica Baiula, Luca Gentilucci, Rossella De Marco, Alessandra Tolomelli

المساهمون: S. D. Dattoli, R. De Marco, M. Baiula, S. Spampinato, A. Greco, A. Tolomelli, L. Gentilucci

المصدر: European Journal of Medicinal Chemistry. 73:225-232

مصطلحات موضوعية: VLA-4 ligands, Protein Conformation, Peptidomimetic, Integrin, β, Anti-Inflammatory Agents, Vascular Cell Adhesion Molecule-1, Integrin alpha4beta1, BETA-AMINO ACID, Isoaspartate, Jurkat Cells, Mice, INFLAMMATION, Drug Stability, Drug Discovery, Cell Adhesion, Animals, Humans, Cell adhesion, Receptor, Nuclear Magnetic Resonance, Biomolecular, Pharmacology, Aspartic Acid, Binding Sites, biology, Chemistry, Cell adhesion inhibition, Organic Chemistry, Cell Adhesion Inhibition, General Medicine, 2, Proline, Diphenylurea, Peptidomimetics, Retro sequences, Scintillation proximity assay, Small molecule, Biochemistry, biology.protein, Oligopeptides, Protein Binding

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6672157650d34d7dcf47e0ca83c3821
https://doi.org/10.1016/j.ejmech.2013.12.009

المؤلفون: Kelly Maurent, Aurélien Lebrun, Emmanuel Aubert, Jean Martinez, Monique Calmes, Claude Didierjean, Pierre Milbeo, Laure Moulat

المساهمون: Institut des Biomolécules Max Mousseron [Pôle Chimie Balard] (IBMM), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Montpellier (UM)-Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM), Cristallographie, Résonance Magnétique et Modélisations (CRM2), Centre National de la Recherche Scientifique (CNRS)-Université de Lorraine (UL)

المصدر: Tetrahedron
Tetrahedron, Elsevier, 2016, 72 (13), pp.1706-1715. ⟨10.1016/j.tet.2016.02.027⟩

مصطلحات موضوعية: chemistry.chemical_classification, Asymmetric aldol reaction, Bicyclic molecule, 010405 organic chemistry, Stereochemistry, Organocatalysis, Carboxylic acid, Organic Chemistry, Absolute configuration, Tripeptide, 010402 general chemistry, 01 natural sciences, Biochemistry, Pyrrolidine, Short alpha/beta-peptide, 0104 chemical sciences, chemistry.chemical_compound, Residue (chemistry), chemistry, Aldol reaction, Drug Discovery, [CHIM.CRIS]Chemical Sciences/Cristallography, Bicyclic beta-amino acid

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3144848b1e1121981a3275fff34a723e
https://hal.univ-lorraine.fr/hal-01532027

المؤلفون: Gunbjørg Svineng, Morten B. Strøm, Dominik Ausbacher, Terkel Hansen

المصدر: Biochimica et Biophysica Acta (BBA) - Biomembranes. 1818:2917-2925

مصطلحات موضوعية: Antimicrobial peptides, Biophysics, Antineoplastic Agents, Apoptosis, Biology, Biochemistry, Cell Line, Membrane Potentials, Flow cytometry, Cell membrane, Inhibitory Concentration 50, Necrosis, chemistry.chemical_compound, Anti-Infective Agents, Microscopy, Electron, Transmission, medicine, Humans, Propidium iodide, chemistry.chemical_classification, medicine.diagnostic_test, Cell Biology, Anticancer peptide, Flow Cytometry, Beta-amino acid, Molecular biology, Mitochondria, Amino acid, medicine.anatomical_structure, chemistry, Cell culture, Caspases, Cancer cell, Microscopy, Electron, Scanning, Antimicrobial peptide, Peptides

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f5ccf272cb5c63459136efe2d59ba93
https://doi.org/10.1016/j.bbamem.2012.07.005

المؤلفون: Yves Chapleur, Anne-Sophie Felten, Manuel Andreini, Nadia Pellegrini-Moïse, Hoang-Trang Tran Thien, Claude Taillefumier

المساهمون: Structure et Réactivité des Systèmes Moléculaires Complexes (SRSMC), Institut de Chimie du CNRS (INC)-Université de Lorraine (UL)-Centre National de la Recherche Scientifique (CNRS), Synthèse et étude de systèmes à intêret biologique (SEESIB), Université Blaise Pascal - Clermont-Ferrand 2 (UBP)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Université de Lorraine (UL)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC), Université Blaise Pascal - Clermont-Ferrand 2 (UBP)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)

المصدر: Tetrahedron Letters
Tetrahedron Letters, 2012, 53, pp.2702-2705. ⟨10.1016/j.tetlet.2012.03.072⟩
Tetrahedron Letters, Elsevier, 2012, 53, pp.2702-2705

مصطلحات موضوعية: chemistry.chemical_classification, animal structures, Stereochemistry, Organic Chemistry, macromolecular substances, beta-amino-acid Aza-beta-peptide C-glycosyl compounds Chiral building block, Biochemistry, Reductive amination, Amino acid, carbohydrates (lipids), chemistry.chemical_compound, chemistry, Drug Discovery, [CHIM]Chemical Sciences, Organic chemistry, lipids (amino acids, peptides, and proteins), Glycosyl

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2bf326878cc5e04c6e5a9b03f8f04f2
https://doi.org/10.1016/j.tetlet.2012.03.072

المؤلفون: Milbeo, Pierre, Maurent, Kelly, Moulat, Laure, Lebrun, Aurelien, Didierjean, Claude, Aubert, Emmanuel, Martinez, Jean, Calmes, Monique

المساهمون: Institut des Biomolécules Max Mousseron Pôle Chimie Balard (IBMM), Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS), Cristallographie, Résonance Magnétique et Modélisations (CRM2), Université de Lorraine (UL)-Centre National de la Recherche Scientifique (CNRS)

المصدر: ISSN: 0040-4020 ; Tetrahedron ; https://hal.univ-lorraine.fr/hal-01532027 ; Tetrahedron, 2016, 72 (13), pp.1706-1715. ⟨10.1016/j.tet.2016.02.027⟩.

مصطلحات موضوعية: Short alpha/beta-peptide, Bicyclic beta-amino acid, Organocatalysis, Asymmetric aldol reaction, [CHIM.CRIS]Chemical Sciences/Cristallography

Relation: hal-01532027; https://hal.univ-lorraine.fr/hal-01532027

الاتاحة: https://hal.univ-lorraine.fr/hal-01532027
https://doi.org/10.1016/j.tet.2016.02.027

المؤلفون: Dao Thi, Hang, Decuyper, Lena, Mollet, Karen, Kenis, Sara, De Kimpe, Norbert, Van Nguyen, Tuyen, D'hooghe, Matthias

المصدر: SYNLETT ; ISSN: 0936-5214

مصطلحات موضوعية: Chemistry, beta-lactams, azetidines, aminopropanes, oxazinanes, fluorine, CF3, BETA-AMINO-ACID, STEREOSELECTIVE-SYNTHESIS, STRAIGHTFORWARD SYNTHESIS, RING TRANSFORMATION, STAUDINGER REACTION, CONTINUOUS-FLOW, HETEROCYCLES, INHIBITORS, PROTEASE, 2-AZETIDINONES

وصف الملف: application/vnd.openxmlformats-officedocument.wordprocessingml.document

Relation: https://biblio.ugent.be/publication/7063602; http://hdl.handle.net/1854/LU-7063602; http://dx.doi.org/10.1055/s-0035-1561316; https://biblio.ugent.be/publication/7063602/file/7069638

الاتاحة: https://biblio.ugent.be/publication/7063602
http://hdl.handle.net/1854/LU-7063602
https://doi.org/10.1055/s-0035-1561316
https://biblio.ugent.be/publication/7063602/file/7069638

المؤلفون: DE MARCO, ROSSELLA, GRECO, ARIANNA, GENTILUCCI, LUCA

المساهمون: Papini, Lubell, R. De Marco, A. Greco, L. Gentilucci

مصطلحات موضوعية: friedinger lactam, beta-amino acid

وصف الملف: STAMPA

Relation: ispartofbook:Abstract Book; PIPS 2014; firstpage:69; lastpage:69; numberofpages:1; alleditors:Papini, Lubell; http://hdl.handle.net/11585/399383

الاتاحة: http://hdl.handle.net/11585/399383