المؤلفون: Wanjun Chen, Xinlong Yan, Lin Fan, Xu Guo, Jian Yang, Yiming Chen, Shaofang Zhou, Guodu Liu

المصدر: Green Synthesis and Catalysis, Vol 5, Iss 4, Pp 282-289 (2024)

مصطلحات موضوعية: All carbon 1,6-alkynone, Ni-catalyzed reductive cyclization, Stereoselective asymmetric catalysis, Cyclopentane with chiral allylic quaternary stereocenter, P-Chiral monophosphine ligand, Chemical technology, TP1-1185, Biochemistry, QD415-436

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2666554923000753; https://doaj.org/toc/2666-5549

URL الوصول: https://doaj.org/article/5e6686a550d3405fbd39bdeedeb77767

المؤلفون: Vladislav Y. Korotaev, Igor B. Kutyashev, Maxim S. Sannikov, Maria A. Mishchenko, Lyudmila S. Zavyalova, Ivan A. Kochnev, Alexey Y. Barkov, Nikolay S. Zimnitskiy, Vyacheslav Y. Sosnovskikh

مصطلحات موضوعية: Biophysics, Biochemistry, Cell Biology, Genetics, Evolutionary Biology, Cancer, Infectious Diseases, Computational Biology, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, similar process involving, ray diffraction analysis, dichlorovinyl )- 5, 2d nmr spectroscopy, pyrrolidines reductive cyclization, mediated reductive cyclization, based reductive systems, tetrahydrochromeno ­[ 3, hexahydrochromeno ­[ 3, 2 -( trihalomethyl, >]­ pyrrole 3, 3 -( 2, >- pyrroline 1, reductive dehalogenation, fused pyrroline, >]­ pyrroles, tunable zinc, reliably confirmed, relative configuration, pyran ring

Relation: https://figshare.com/articles/journal_contribution/Tunable_Zinc-Mediated_Reductive_Cyclization_of_Diastereomeric_3_Nitro-4-phenacyl-2-_trihalomethyl_chromanes_to_Fused_Pyrroline_i_N_i_Oxides_Pyrrolines_and_Pyrrolidines/25035614

الاتاحة: https://doi.org/10.1021/acs.joc.3c02191.s001
https://figshare.com/articles/journal_contribution/Tunable_Zinc-Mediated_Reductive_Cyclization_of_Diastereomeric_3_Nitro-4-phenacyl-2-_trihalomethyl_chromanes_to_Fused_Pyrroline_i_N_i_Oxides_Pyrrolines_and_Pyrrolidines/25035614

المؤلفون: Fraga, Guido Gustavo

مصطلحات موضوعية: Química, 1-nitro-2-naftaldehído, 2-cloroacetamidas, ciclización reductiva, rmn, 1-nitro-2-naphtaldehyde, 2-chloroacetamides, reductive cyclization, nmr

وصف الملف: application/pdf

Relation: http://sedici.unlp.edu.ar/handle/10915/173262

الاتاحة: http://sedici.unlp.edu.ar/handle/10915/173262

المؤلفون: Sudip Bhattacharjee, Anjana Tripathi, Rupak Chatterjee, Ranjit Thapa, Thomas E. Mueller, Asim Bhaumik

مصطلحات موضوعية: Biochemistry, Molecular Biology, Sociology, Inorganic Chemistry, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, two porous polymers, showed good yields, reductive cyclization reactions, methanol via hydrosilylation, low energy barrier, exhibited outstanding stability, high surface area, 02 , selectively reduced co, 85 mmol g, 0 bar pressure, conversion reaction due, 2 , 2 , 01 , complete conversion, high flexibility, high co, n <, useful chemicals, uptake capacity, steady rise, reaction mechanisms

Relation: https://figshare.com/articles/journal_contribution/_i_N_i_Heterocyclic_Carbene_Moiety_in_Highly_Porous_Organic_Hollow_Nanofibers_for_Efficient_CO_sub_2_sub_Conversions_A_Comparative_Experimental_and_Theoretical_Study/24925774

الاتاحة: https://doi.org/10.1021/acscatal.3c05576.s001
https://figshare.com/articles/journal_contribution/_i_N_i_Heterocyclic_Carbene_Moiety_in_Highly_Porous_Organic_Hollow_Nanofibers_for_Efficient_CO_sub_2_sub_Conversions_A_Comparative_Experimental_and_Theoretical_Study/24925774

المؤلفون: Sayan Pramanik, Chhanda Mukhopadhyay

المصدر: Beilstein Journal of Organic Chemistry, Vol 18, Iss 1, Pp 469-478 (2022)

مصطلحات موضوعية: chemoselective conjugate reduction, dispirocyclopentanebisoxindole scaffolds, metal-free, one-pot operation, reductive cyclization, Science, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1860-5397

URL الوصول: https://doaj.org/article/4fcbe2490b6049af9ce7521ea77f9456

المؤلفون: Evgeny V. Pospelov, Alexey Yu. Sukhorukov

المصدر: International Journal of Molecular Sciences; Volume 24; Issue 14; Pages: 11794

مصطلحات موضوعية: piperazines, reductive cyclization, Michael addition, oximes, heterogeneous catalytic hydrogenation

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Molecular Pharmacology; https://dx.doi.org/10.3390/ijms241411794

الاتاحة: https://doi.org/10.3390/ijms241411794

المؤلفون: Sirvinskaite, Giedre, Nardo, Celine S., Müller, Patrick, id_orcid:0 000-0001-7253-7198, Gasser, Aurelio C., Morandi, Bill

المصدر: Chemistry - A European Journal, 29 (54)

مصطلحات موضوعية: Amination, nitrene source, nitroarenes, reductive cyclization, unprotected indolines

وصف الملف: application/application/pdf

Relation: info:eu-repo/semantics/altIdentifier/wos/001051455900001; info:eu-repo/grantAgreement/SNF/Projekte MINT/184658; http://hdl.handle.net/20.500.11850/628622

الاتاحة: https://hdl.handle.net/20.500.11850/628622
https://doi.org/10.3929/ethz-b-000628622

المؤلفون: Ramadan D. R., Ferretti F., Ragaini F.

المساهمون: D.R. Ramadan, F. Ferretti, F. Ragaini

مصطلحات موضوعية: 9H-carbazole, Carbon monoxide surrogate, Nitrobiphenyl, Palladium, Phenyl formate, Reductive cyclization, Settore CHIM/03 - Chimica Generale e Inorganica, Settore CHIM/06 - Chimica Organica

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000807512800005; volume:409; firstpage:41; lastpage:47; numberofpages:7; journal:JOURNAL OF CATALYSIS; https://hdl.handle.net/2434/923370; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85127474062

الاتاحة: https://hdl.handle.net/2434/923370
https://doi.org/10.1016/j.jcat.2022.03.024

المؤلفون: Uludağ, Nesimi, Üstun, Elvan, Serdaroğlu, Goncagül

مصطلحات موضوعية: Uleine, Noruleine, Alzheimer's disease, DFT computations, Molecular dockings, Concise Total-Synthesis, Reductive Cyclization Route, Human Serum-Albumin, Ft-Ir, Crystal-Structure, Orbital Methods, Ab-Initio, Basis-Set, Drug, Framework

Relation: Heliyon; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://doi.org/10.1016/j.heliyon.2022.e11990; https://hdl.handle.net/20.500.11776/11954; 12; WOS:000904031300016; 2-s2.0-85144046729

الاتاحة: https://hdl.handle.net/20.500.11776/11954
https://doi.org/10.1016/j.heliyon.2022.e11990

المؤلفون: Folgueiras-Amador, AA, Teuten, AE, Salam-Perez, M, Pearce, JE, Denuault, G, Pletcher, D, Parsons, PJ, Harrowven, DC, Brown, RCD

مصطلحات موضوعية: Science & Technology, Physical Sciences, Chemistry, Multidisciplinary, Electrosynthesis, Flow Chemistry, Mediator, Radical Cyclization, Reductive Cyclization, STATE LIMITING CURRENTS, ELECTROCHEMICAL REDUCTION, ELECTROLYSIS CELL, EC PROCESSES, MICROELECTRODE, KINETICS, LIGHT, COMPLEXES, MECHANISM, Organic Chemistry, 03 Chemical Sciences

Relation: Angewandte Chemie International Edition; http://hdl.handle.net/10044/1/98509

الاتاحة: http://hdl.handle.net/10044/1/98509
https://doi.org/10.1002/anie.202203694

المساهمون: Qu, Wenchao [Brookhaven National Lab. (BNL), Upton, NY (United States). Biological, Environmental & Climate Sciences Department]

المصدر: Organic and Biomolecular Chemistry; 13; 46

وصف الملف: Medium: ED; Size: p. 11235 - 11243

URL الوصول: http://www.osti.gov/scitech/servlets/purl/1239796

المؤلفون: Reshma Sathyanarayana, Boja Poojary

المصدر: Molbank, Vol 2021, Iss 1, p M1192 (2021)

مصطلحات موضوعية: benzimidazole, nitro-reductive cyclization, UV-Vis, photoluminescence, CV, TGA, Inorganic chemistry, QD146-197

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-8599/2021/1/M1192; https://doaj.org/toc/1422-8599

URL الوصول: https://doaj.org/article/df6203caa45d4d7e9eca651ef0a71514

المؤلفون: Kanchani, Janardhanreddy, M.C.S., Subha

المصدر: DER PHARMA CHEMICA, 13(3), 3, (2021-05-22)

مصطلحات موضوعية: Miyaura coupling, Bispinacolatodiboron, TetrakisdiphenylphosphinoPd catalyst, Triphenyl phosphine, Cadagon reductive cyclization

Relation: https://doi.org/10.5281/zenodo.11070903; https://doi.org/10.5281/zenodo.11070904; oai:zenodo.org:11070904

الاتاحة: https://doi.org/10.5281/zenodo.11070904

المؤلفون: Shengquan Duan (1857154), Daniel W. Widlicka (1413220), Michael P. Burns (11382574), Rajesh Kumar (72124), Ian Hotham (11382577), Jean-Nicolas Desrosiers (1392826), Paul Bowles (1458148), Kris N. Jones (1857169), Lindsay D. Nicholson (11382580), Michele T. Buetti-Weekly (11382583), Lu Han (151620), Jeremy Steflik (1292913), Eric Hansen (2337007), Cheryl M. Hayward (1997578), Holly Strohmeyer (1857070), Sébastien Monfette (11382586), Scott C. Sutton (2025337), Christopher Morris (92583)

مصطلحات موضوعية: Biochemistry, Molecular Biology, Pharmacology, Biotechnology, Marine Biology, Infectious Diseases, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, substituted chiral amines, enzymatic reductive amination, engineered imine reductase, chiral secondary amine, catalyzed reductive cyclization, biocatalytic reductive amination, n , 3 , process development, powerful tool, key intermediate, high diastereoselectivity, cdk 2, also presented, 6 inhibitor

Relation: https://figshare.com/articles/journal_contribution/Application_of_Biocatalytic_Reductive_Amination_for_the_Synthesis_of_a_Key_Intermediate_to_a_CDK_2_4_6_Inhibitor/16566430

الاتاحة: https://doi.org/10.1021/acs.oprd.1c00255.s001

المؤلفون: Nicole A. Carrillo Vallejo (10519282), Jonathan R. Scheerer (1676254)

مصطلحات موضوعية: Biochemistry, Molecular Biology, Pharmacology, Hematology, Infectious Diseases, Computational Biology, Space Science, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Oxazinone, Alkyne substrates, ErbB 4 receptor inhibitor, Pyridine Derivatives, Tandem, oxazinone derivatives, functionalized vinyl azide precursors, regioselectivity, sequence, application, Construction, method, terminal alkyne substrates, synthesis, Precursor, Staudinger reductive cyclization, propargyl oxygen substitution, cycloaddition operation, polysubstituted pyridine products, preparation, Cycloaddition

Relation: https://figshare.com/articles/journal_contribution/Application_of_1_4-Oxazinone_Precursors_to_the_Construction_of_Pyridine_Derivatives_by_Tandem_Intermolecular_Cycloaddition_Cycloreversion/14363656

الاتاحة: https://doi.org/10.1021/acs.joc.1c00288.s001

المؤلفون: ABDELLATIF, MANAR AHMED FOUAD

المساهمون: tutor: F. A. C. Ragaini, coordinator: D. Passarella, M.A.F. Abdellatif, RAGAINI, FABIO ATTILIO CIRILLO, PASSARELLA, DANIELE

مصطلحات موضوعية: Reductive Cyclization, Reduction, Palladium, Catalysi, Heterocycle, CO, Formic Acid, Phenyl Formate, Formate Ester, Indole, Quinolone, Oxazine, Pyrrole, Nitro compounds

Relation: https://hdl.handle.net/2434/1026030

الاتاحة: https://hdl.handle.net/2434/1026030

المؤلفون: Raghuram Gujjarappa, Nagaraju Vodnala, Arup K. Kabi, Dhananjaya Kaldhi, Mohan Kumar, Uwe Beifuss, Chandi C. Malakar

المصدر: SynOpen, Vol 02, Iss 02, Pp 0138-0144 (2018)

مصطلحات موضوعية: n-heterocycles, domino reaction, reductive cyclization, nitro­arenes, dioxo-mo(vi) complex, pinacol, Chemistry, QD1-999

وصف الملف: electronic resource

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

URL الوصول: https://doaj.org/article/623d494ec0874b729300e8f7b25f70d2

المؤلفون: Prakash Bhaskar, Vasantha Kumar, Suresha Kumara Tholappanavara Hanumanthappa, Sowmya Haliwana Banakara Vijaykumar

المصدر: Molbank, Vol 2019, Iss 3, p M1079 (2019)

مصطلحات موضوعية: benzimidazole, carboxamide, one-pot synthesis, reductive cyclization, Inorganic chemistry, QD146-197

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-8599/2019/3/M1079; https://doaj.org/toc/1422-8599

URL الوصول: https://doaj.org/article/eb6de30929ed4e82a7c033c4e3e51dcd

المؤلفون: Yoshio Ando, 安藤 吉勇

المصدر: 有機合成化学協会誌 / Journal of Synthetic Organic Chemistry, Japan. 2020, 78(4):304

المؤلفون: Miguel Claros, Felix Ungeheuer, Federico Franco, Vlad Martin‐Diaconescu, Alicia Casitas, Julio Lloret‐Fillol

المساهمون: Claros, Miguel, Ungeheuer, Felix, Franco, Federico, Martin‐diaconescu, Vlad, Casitas, Alicia, Lloret‐fillol, Julio

مصطلحات موضوعية: Reductive Cyclization, Unactivated Alkyl Chloride, Visible-Light Photoredox Catalysis

Relation: info:eu-repo/semantics/altIdentifier/pmid/30707782; info:eu-repo/semantics/altIdentifier/wos/WOS:000463739900010; volume:131/2019; issue:15; firstpage:4923; lastpage:4928; numberofpages:6; journal:ANGEWANDTE CHEMIE; https://hdl.handle.net/11368/3044369; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85062801632

الاتاحة: https://hdl.handle.net/11368/3044369
https://doi.org/10.1002/ange.201812702
https://onlinelibrary.wiley.com/doi/10.1002/ange.201812702