المؤلفون: Söderberg, Elisabeth, von Borries, Kerstin, Norinder, Ulf, Petchey, Mark, Ranjani, Ganapathy, Chavan, Swapnil, 1986, Holmquist, Hanna, Johansson, Magnus, Cotgreave, Ian, Hayes, Martin A., Fantke, Peter, Syrén, Per-Olof

المصدر: Green Chemistry. 26(22):11147-11163

مصطلحات موضوعية: Sustainable chemistry, Synthesis (chemical), Amide bond, Bond coupling, Bond-forming reactions, Building blockes, Chemistry research, Green-chemistry, Human toxicity, In-silico, Research areas, Synthetases, Biocatalysts

وصف الملف: electronic

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:ri:diva-76006
https://doi.org/10.1039/d4gc03665d
https://ri.diva-portal.org/smash/get/diva2:1913152/FULLTEXT01.pdf

المؤلفون: Rouge, Elisa, Brunel, Jean, Michel

المساهمون: Membranes et cibles thérapeutiques (MCT), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Recherche Biomédicale des Armées Brétigny-sur-Orge (IRBA)

المصدر: ISSN: 0040-4020 ; Tetrahedron ; https://hal.science/hal-04736531 ; Tetrahedron, 2024, 151, ⟨10.1016/j.tet.2023.133813⟩.

مصطلحات موضوعية: Amide bond formation Peptide coupling Microwave reaction Propylphosphonic anhydride, Amide bond formation -Peptide coupling -Microwave reactionpropylphosphonic anhydride, [CHIM]Chemical Sciences

الاتاحة: https://hal.science/hal-04736531
https://hal.science/hal-04736531v1/document
https://hal.science/hal-04736531v1/file/Manuscript%20Tetrahedron%20brunel%20et%20al.pdf
https://doi.org/10.1016/j.tet.2023.133813

المؤلفون: Jeesoo Choi, Anna Nawachi, Natsuki Saito, Yuta Kondo, Hiroyuki Morimoto, Takashi Ohshima

المصدر: Frontiers in Chemistry, Vol 12 (2024)

مصطلحات موضوعية: amide bond cleavage, functional group compatibility, functional group evaluation kit, carboxylic acid, zinc trifluoromethanesulfonate, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fchem.2024.1378746/full; https://doaj.org/toc/2296-2646

URL الوصول: https://doaj.org/article/5b071709d2694d959aefd26b4b710b18

المؤلفون: Ruiqi Piao, Yong-Uk Kwon

المصدر: International Journal of Molecular Sciences ; Volume 25 ; Issue 21 ; Pages: 11390

مصطلحات موضوعية: amide bond cleavage, conformational effect, electronic effect, N -acylated peptoid, n → π * interaction

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Biochemistry; https://dx.doi.org/10.3390/ijms252111390

الاتاحة: https://doi.org/10.3390/ijms252111390

المؤلفون: Choudhuri, Khokan, Zhang, Zhenguo, Loh, Teck-Peng

المساهمون: School of Chemistry, Chemical Engineering and Biotechnology

مصطلحات موضوعية: Chemistry, Alkynoates, Amide bond formation

وصف الملف: application/pdf

Relation: M21K2c0114; M22K9b0049; Science Advances; https://hdl.handle.net/10356/180454; 38; 10; eadp7544

الاتاحة: https://hdl.handle.net/10356/180454
https://doi.org/10.1126/sciadv.adp7544

المؤلفون: Qingyun Tang, Mark Petchey, Benjamin Rowlinson, Thomas J. Burden, Ian J. S. Fairlamb, Gideon Grogan

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Pharmacology, Biotechnology, Chemical Sciences not elsewhere classified, subsequent amidation using, revealing key roles, ray crystallographic structure, permitted mutational mapping, frequently performed reactions, form amine products, amine binding sites, amide bond synthetases, previously studied abs, amine coupling partners, contemporary pharmaceutical synthesis, carboxylic acid substrates, amine substrates, carboxylic acid, coupling agents, amine partner, amine nucleophile, amide bonds, pharmaceutical synthesis, activated substrates, racemic acid, chiral acid, streptoalloteichus hindustanus, stoichiometric quantities

Relation: https://figshare.com/articles/journal_contribution/Broad_Spectrum_Enantioselective_Amide_Bond_Synthetase_from_Streptoalloteichus_hindustanus/24953739

الاتاحة: https://doi.org/10.1021/acscatal.3c05656.s001
https://figshare.com/articles/journal_contribution/Broad_Spectrum_Enantioselective_Amide_Bond_Synthetase_from_Streptoalloteichus_hindustanus/24953739

المؤلفون: Brice A. Ludwig, Christina R. Forbes, Neal J. Zondlo

مصطلحات موضوعية: Biophysics, Biochemistry, Genetics, Molecular Biology, Infectious Diseases, Chemical Sciences not elsewhere classified, mechanistic insights lead, computational investigations indicated, using inexpensive boc, mercaptoproline proceeded slowly, mercaptoproline proceeded efficiently, standard ncl conditions, native amide bond, forward reaction ), fully synthesized peptides, >- acyl intermediate, ncl using mercaptoproline, peptides containing n, n , >- mercaptoproline, terminal boc, synthesized directly, acyl transfer, ncl reactions, n <, functionalized n, >- hydroxyproline, >- bromoproline, without epimerization, transition states

Relation: https://figshare.com/articles/journal_contribution/N_Terminal_Proline_Editing_for_the_Synthesis_of_Peptides_with_Mercaptoproline_and_Selenoproline_Mechanistic_Insights_Lead_to_Greater_Efficiency_in_Proline_Native_Chemical_Ligation/25180518

الاتاحة: https://doi.org/10.1021/acschembio.3c00705.s001
https://figshare.com/articles/journal_contribution/N_Terminal_Proline_Editing_for_the_Synthesis_of_Peptides_with_Mercaptoproline_and_Selenoproline_Mechanistic_Insights_Lead_to_Greater_Efficiency_in_Proline_Native_Chemical_Ligation/25180518

المؤلفون: Fairchild, Jasper, Islam, Saidul, Singh, Jyoti, Bučar, Dejan-Krešimir, Powner, Matthew W.

المصدر: Fairchild , J , Islam , S , Singh , J , Bučar , D-K & Powner , M W 2024 , ' Prebiotically plausible chemoselective pantetheine synthesis in water ' , Science , vol. 383 , no. 6685 , pp. 911-918 . https://doi.org/10.1126/science.adk4432

مصطلحات موضوعية: Chemistry, Prebiotic chemistry, Origin of life, Metabolism, Pantetheine, Coenzyme A, ALDOL REACTIONS, Amide bond, Nitrile, Aminonitrile, Cyanide, Protometabolism

وصف الملف: application/pdf

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/145d5179-89c0-4955-932e-ad619db3e41a
https://doi.org/10.1126/science.adk4432
https://kclpure.kcl.ac.uk/ws/files/253852345/Islam_Pantetheine_accept.pdf
http://www.scopus.com/inward/record.url?scp=85185901425&partnerID=8YFLogxK

المؤلفون: Aravinda Babu, Kenchaiah Sunil, Ayyiliath Meleveetil Sajith, Eeda Koti Reddy, Sougata Santra, Grigory V. Zyryanov, Talavara Venkatesh, Somashekara Bhadrachari, Muthipeedika Nibin Joy

المصدر: Pharmaceuticals, Vol 17, Iss 5, p 548 (2024)

مصطلحات موضوعية: dihydrotriazolopyrimidine, N -methylimidazole, sulfuryl chloride, amide bond formation, anti-inflammatory activity, anti-tubercular activity, Medicine, Pharmacy and materia medica, RS1-441

Relation: https://www.mdpi.com/1424-8247/17/5/548; https://doaj.org/toc/1424-8247; https://doaj.org/article/896784a67c514216aae7250c250976a3

الاتاحة: https://doi.org/10.3390/ph17050548
https://doaj.org/article/896784a67c514216aae7250c250976a3

المؤلفون: Koichi Fukase, Yoshiyuki Manabe, Atsushi Shimoyama

المصدر: Frontiers in Chemistry, Vol 11 (2023)

مصطلحات موضوعية: glycosylation, amide bond, amide, oligosaccharide, glycan, flow reaction, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fchem.2023.1319883/full; https://doaj.org/toc/2296-2646

URL الوصول: https://doaj.org/article/5ebb81c9a4e849658021adfb4922022a

المؤلفون: Chengwei Liu, Michal Szostak

المصدر: SynOpen, Vol 07, Iss 01, Pp 88-101 (2023)

مصطلحات موضوعية: C–N activation, amide bond activation, acyl coupling, decarbonylative coupling, acyl addition, catalysis, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2509-9396

URL الوصول: https://doaj.org/article/de252149b71c48c285240276e9bfb2eb

المؤلفون: Chika Azuma, Haydar Bulut, Hiroaki Mitsuya, Hirokazu Tamamura, Kenichi Yamamoto, Kohei Tsuji, Kouki Shinohara, Nobuyo Higashi-Kuwata, Shin-ichiro Hattori, Soshi Nishimura, Takahiro Ishii, Takuya Kobayakawa, Yutaro Miura

المصدر: Chemical and Pharmaceutical Bulletin. 2023, 71(12):879

المؤلفون: Nikolay G. Vassilev, Ivo C. Ivanov

المصدر: Molecules, Vol 28, Iss 24, p 8004 (2023)

مصطلحات موضوعية: rotational barrier energy, amide bond, enamine bond, dynamic NMR, reference deconvolution, DFT calculations, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1420-3049/28/24/8004; https://doaj.org/toc/1420-3049

URL الوصول: https://doaj.org/article/979f8b6db67b4404a05aac3fba31cfd2

المؤلفون: Naoyuki Shimada, 嶋田 修之

المصدر: 有機合成化学協会誌 / Journal of Synthetic Organic Chemistry, Japan. 2023, 81(7):668

المؤلفون: Rakshit Kumar Jain, Carol K. Hall, Erik E. Santiso

مصطلحات موضوعية: Biophysics, Biochemistry, Space Science, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, Information Systems not elsewhere classified, secondary structures owing, possible side chains, parallel bias metadynamics, important step toward, four side chains, complete energy landscapes, tempered metadynamics simulations, previously available collection, complex conformational landscape, peptoid amide bond, ab initio <, available experimental data, >) peptoid monomers, experimental data, diverse collection, conformational space, atomistic simulations, trans <, s1pe <, s1ne <, cis <, work represents, wide variety

Relation: https://figshare.com/articles/journal_contribution/Using_Enhanced_Sampling_Simulations_to_Study_the_Conformational_Space_of_Chiral_Aromatic_Peptoid_Monomers/24525067

الاتاحة: https://doi.org/10.1021/acs.jctc.3c00803.s002
https://figshare.com/articles/journal_contribution/Using_Enhanced_Sampling_Simulations_to_Study_the_Conformational_Space_of_Chiral_Aromatic_Peptoid_Monomers/24525067

المؤلفون: Jeffrey J. Jackson, Aaron C. Siegmund, Wen-Ju Bai, Anthony B. Reed, Adam B. Birkholz, Iain D. G. Campuzano, Amandine Créquer-Grandhomme, Ruozhen Hu, Rucha V. Modak, Athena Sudom, Noelle Javier, Christiana Sanders, Mei-Chu Lo, Fang Xie, Victor J. Cee, Paolo Manzanillo, John G. Allen

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Pharmacology, Immunology, Developmental Biology, Mental Health, Hematology, Chemical Sciences not elsewhere classified, β ‑ 1, ray cocrystal structures, cell surface long, based drug design, >‑ acetylglucosaminyltransferase 2, vivo <, successfully serve, pk properties, pharmacokinetic properties, n <, isoform selectivity, improved potency, immune response, chain polylactosamine, certain physicochemical, attractive target, amide bond, amide bioisosteres, amide bioisostere, 3 ‑<

Relation: https://figshare.com/articles/journal_contribution/Imidazolone_as_an_Amide_Bioisostere_in_the_Development_of_1_3_i_N_i_Acetylglucosaminyltransferase_2_B3GNT2_Inhibitors/24602242

الاتاحة: https://doi.org/10.1021/acs.jmedchem.3c01517.s001
https://figshare.com/articles/journal_contribution/Imidazolone_as_an_Amide_Bioisostere_in_the_Development_of_1_3_i_N_i_Acetylglucosaminyltransferase_2_B3GNT2_Inhibitors/24602242

المؤلفون: Simon J. Shaw, Dane A. Goff, Luke A. Boralsky, Rajinder Singh, David J. Sweeny, Gary Park, Tian-Qiang Sun, Yonchu Jenkins, Vadim Markovtsov, Sarkiz D. Issakani, Donald G. Payan, Yasumichi Hitoshi

مصطلحات موضوعية: Biochemistry, Cell Biology, Genetics, Physiology, Pharmacology, Developmental Biology, Cancer, Chemical Sciences not elsewhere classified, type ii diabetes, secondary amide bond, lowering fasted glucose, inhibiting amide hydrolysis, vitro safety profile, liver blood flow, reduced rat clearance, db mouse model, 32 , rat clearance, mouse liver, trans <, herg profile, target potency, strategic placement, steric environment, position 3, piperidine ring, piperidine moiety, oral dosing, insulin levels, generated around

Relation: https://figshare.com/articles/journal_contribution/Optimization_of_Pharmacokinetic_and_In_Vitro_Safety_Profile_of_a_Series_of_Pyridine_Diamide_Indirect_AMPK_Activators/24790501

الاتاحة: https://doi.org/10.1021/acs.jmedchem.3c01983.s001
https://figshare.com/articles/journal_contribution/Optimization_of_Pharmacokinetic_and_In_Vitro_Safety_Profile_of_a_Series_of_Pyridine_Diamide_Indirect_AMPK_Activators/24790501

المؤلفون: Rowlinson, Michael, Micklefield, Jason

المصدر: Rowlinson , M & Micklefield , J 2023 , ' Biocatalytic Approaches to Amide Synthesis ' , Comprehensive Chirality . https://doi.org/10.1016/B978-0-32-390644-9.00083-4

مصطلحات موضوعية: Adenylate, Amide, Amide bond synthetase, ATP-grasp, Biocatalyst, Biosynthesis, Catalysis, Coenzyme A-ligase, Hydrate, Hydrolytic, Lipase, N-acyltransferases, Nitrile hydratase, Phosphorylate, One-pot

الاتاحة: https://research.manchester.ac.uk/en/publications/426fa5b4-2506-43bb-acc7-f12c635f90bb
https://doi.org/10.1016/B978-0-32-390644-9.00083-4

المؤلفون: Satenik Mkrtchyan (1651666), Mohanad Shkoor (3768385), Mandalaparthi Phanindrudu (4418992), Miroslav Medved′ (1772632), Olena Sevastyanova (3125073), Viktor O. Iaroshenko (1348473)

مصطلحات موضوعية: Biophysics, Biochemistry, Cell Biology, Genetics, Molecular Biology, Neuroscience, Biotechnology, Evolutionary Biology, Mental Health, Infectious Diseases, Plant Biology, Chemical Sciences not elsewhere classified, previously reported methods, mechanochemically induced reaction, either arylboronic acids, c – cf, amide synthetic methods, 3 , 2 , mechanochemical defluorinative arylation, substituted aromatic amides, defluorinative arylation, aromatic amides, amide bond, wide variety, wide array, various fields, underexplored strategy, sulfonium salts, scalable routes

Relation: https://figshare.com/articles/journal_contribution/Mechanochemical_Defluorinative_Arylation_of_Trifluoroacetamides_An_Entry_to_Aromatic_Amides/21843230

الاتاحة: https://doi.org/10.1021/acs.joc.2c02197.s001

المؤلفون: Mouna El Khabchi, Mohammed Mcharfi, Mohammed Benzakour, Asmae Fitri, Adil Touimi Benjelloun, Jong-Won Song, Kang-Bong Lee, Ho-Jin Lee

المصدر: Molecules; Volume 28; Issue 14; Pages: 5454

مصطلحات موضوعية: azapeptides, conformational preferences, hydrogen bonds, cis-trans amide bond, β-turn, Asx turn, density functional theory

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: https://dx.doi.org/10.3390/molecules28145454

الاتاحة: https://doi.org/10.3390/molecules28145454