المؤلفون: Chou-Yi Hsu, Riyadh Abdulkareem, Harikumar Pallathadka, Vikrant Abbot, Mamata Chahar, Dilsora Abduvalieva, Yasser Fakri Mustafa, Usama S. Altimari, Abeer mhussan jabbar, Ahmed Hussein Zwamel

المصدر: Scientific Reports, Vol 14, Iss 1, Pp 1-12 (2024)

مصطلحات موضوعية: Dibenzo-chromeno-phenazine-diones. Multicomponent domino reactions (MCDRs). 1,3-n-propyl-bipyridinium bisulfonic acid-ditrifluoroacetate (PBPBSDT). Solvent-free medium, Medicine, Science

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2045-2322

URL الوصول: https://doaj.org/article/0a443d91618a49d4b8c20ab0eeee4644

المؤلفون: Malahat Kurbanova, Suraj N. Mali, Fidan Gurbanova, Haya Yasin, Shailesh S. Gurav, Chin-Hung Lai

المصدر: Chemical Physics Impact, Vol 9, Iss , Pp 100716- (2024)

مصطلحات موضوعية: Spirobi[hexahidropyrimidine]-diones derivative, X-ray analysis, Molecular docking, ADME, DFT, Physics, QC1-999, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2667022424002603; https://doaj.org/toc/2667-0224

URL الوصول: https://doaj.org/article/8a88282052084ad59a20e09d5e420c72

المؤلفون: Fatemeh Molaei Yielzoleh, Kobra Nikoofar

المصدر: Scientific Reports, Vol 14, Iss 1, Pp 1-16 (2024)

مصطلحات موضوعية: Spinel FeAl2O4, DL-alanine, Ionic liquid (IL), Spiro[chromeno[2,3-c]pyrazole-4,2′-indene]triones, Spiro[chromeno[2,3-c]pyrazole-4,3′-indoline]diones, Domino reaction, Medicine, Science

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2045-2322

URL الوصول: https://doaj.org/article/cd58b32707e2418a9a4236fedcfb4ab9

المؤلفون: Sami Chniti, Péter Pongrácz, László Kollár, Attila Bényei, Ágnes Dörnyei, Attila Takács

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Molecular Biology, Biotechnology, Evolutionary Biology, Immunology, Chemical Sciences not elsewhere classified, undergo anrorc rearrangement, procedure successfully provided, crystal xrd analysis, bidentate phosphine ligands, stage carbonyl insertion, diones via ring, carbonyl source, using monodentate, undoubtedly established, two types, state structures, secondary amines, reaction toward, michael addition, last ring, isolated yields, favored concomitantly, closure step, catalyzed aminocarbonylation, catalytic cycle, carbonylated compounds, carbon monoxide

Relation: https://figshare.com/articles/journal_contribution/Synthesis_of_Chroman-2_4-diones_via_Ring-Opening_Ring-Closing_Reaction_Involving_Palladium-Catalyzed_Intramolecular_Aryloxycarbonylation/24968996

الاتاحة: https://doi.org/10.1021/acs.joc.3c02337.s001
https://figshare.com/articles/journal_contribution/Synthesis_of_Chroman-2_4-diones_via_Ring-Opening_Ring-Closing_Reaction_Involving_Palladium-Catalyzed_Intramolecular_Aryloxycarbonylation/24968996

المؤلفون: Zongli Xiong, Fuxing Xu, Yuqiao Zhou, Rong Zhang, Yulong Zhang, Yushuang Chen, Weijun Yao, Zhen Wang

مصطلحات موضوعية: Ecology, Sociology, Immunology, Developmental Biology, Plant Biology, Environmental Sciences not elsewhere classified, broad substrate scope, c rearrangement products, >)- ones enabled, ‑ c rearrangement, c rearrangement, wide range, strategy tolerated, quaternary stereocenter, h <, enantioselective construction, efficient asymmetric, diones containing, copper complex, chiral bisoxazoline, also realized

Relation: https://figshare.com/articles/journal_contribution/Enantioselective_Construction_of_C4-Quaternary_Quinolinones_via_Copper_II_-Catalyzed_Asymmetric_1_3_O_to_C_Rearrangement/24565717

الاتاحة: https://doi.org/10.1021/acs.orglett.3c03378.s001
https://figshare.com/articles/journal_contribution/Enantioselective_Construction_of_C4-Quaternary_Quinolinones_via_Copper_II_-Catalyzed_Asymmetric_1_3_O_to_C_Rearrangement/24565717

المؤلفون: Vakhid A. Mamedov, Venera R. Galimullina, Zheng-Wang Qu, Hui Zhu, Victor V. Syakaev, Leisan R. Shamsutdinova, Mikhail A. Sergeev, Il’dar Kh. Rizvanov, Aidar T. Gubaidullin, Oleg G. Sinyashin, Stefan Grimme

مصطلحات موضوعية: Biochemistry, Medicine, Cell Biology, Genetics, Molecular Biology, Ecology, Developmental Biology, Cancer, Inorganic Chemistry, Plant Biology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, quite mild conditions, extensive dft calculations, direct intramolecular indolinone, 3 ′- diones, throughput screening, readily available, reaction mechanism, quinolone rearrangement, medicinal chemistry, easy access, diverse library, could potentially, b <, >] quinoxalin, 4 ‑<, 4 -<

Relation: https://figshare.com/articles/journal_contribution/AlCl_sub_3_sub_Promoted_Intramolecular_Indolinone-Quinolone_Rearrangement_of_Spiro_indoline-3_2_-quinoxaline_-2_3_-diones_Easy_Access_to_Quinolino_3_4_i_b_i_quinoxalin-6-ones/24911061

الاتاحة: https://doi.org/10.1021/acs.joc.3c01906.s002
https://figshare.com/articles/journal_contribution/AlCl_sub_3_sub_Promoted_Intramolecular_Indolinone-Quinolone_Rearrangement_of_Spiro_indoline-3_2_-quinoxaline_-2_3_-diones_Easy_Access_to_Quinolino_3_4_i_b_i_quinoxalin-6-ones/24911061

المؤلفون: Maxim Stanislavovich Kazunin, Oleksii Yurievich Voskoboynik, Svetlana Valentynivna Shishkina, Oleksii Mykolayovych Antypenko, Sergey Ivanovich Kovalenko

المصدر: Acta Chimica Slovenica, Vol 67, Iss 2, Pp 586-593 (2020)

مصطلحات موضوعية: 1-methyl-6-(2-oxo-2-arylethyl)pteridine-2,4,7(1h,3h,8h)-triones, dehydration, 1-methyl-7-arylfuro[3,2-g]pteridine-2,4(1h,3h)diones, alkylation, x-ray diffraction analysis, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://journals.matheo.si/index.php/ACSi/article/view/5601; https://doaj.org/toc/1318-0207; https://doaj.org/toc/1580-3155

URL الوصول: https://doaj.org/article/aeb4d18a9ee84d00bb4ee43231adf054

المؤلفون: Ayambekam Fazilat, Ghashang Majid

المصدر: Main Group Metal Chemistry, Vol 43, Iss 1, Pp 77-83 (2020)

مصطلحات موضوعية: quinazoline-2,4(1h,3h)-diones, na2sio3, snfe2o4 nano-particles, benzo[i]quinazoline, pyrano [3,4-i]quinazoline, thiopyrano[3,4-i]quinazoline, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://doaj.org/toc/0792-1241; https://doaj.org/toc/2191-0219

URL الوصول: https://doaj.org/article/5bab66710b5d49889ce9ab1284ebc755

المؤلفون: Abdulaziz Abdullah Qasem Ali, Mohd Umar Khan, Zeba N. Siddiqui

المصدر: Current Research in Green and Sustainable Chemistry, Vol 5, Iss , Pp 100231- (2022)

مصطلحات موضوعية: CuO-MoO3@PEG, Heterogeneous catalysis, Poly ethylene glycol-6000, Pyrimidine diones, Enamination, Dimedone, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2666086521001788; https://doaj.org/toc/2666-0865

URL الوصول: https://doaj.org/article/e7f7373c62bd41d284693968212d5640

المؤلفون: Majid Mommahed Heravi (9225485), Mansoureh Daraie (6995462)

مصطلحات موضوعية: Organic Chemistry, Nuclear Chemistry, Non-metal Chemistry, Nanochemistry and Supramolecular Chemistry, Optical Properties of Materials, Natural Products Chemistry, Organic Green Chemistry, Organic Chemistry not elsewhere classified, Quantum Chemistry, Organometallic Chemistry, pyrazolo[41,31:5,6]pyrido[2,3-d]pyrimidine-diones, green synthesis, multi-component, reaction, in water reaction

Relation: https://figshare.com/articles/journal_contribution/A_Novel_and_Efficient_Five-Component_Synthesis_of_Pyrazole_Based_Pyrido_2_3-d_pyrimidine-diones_in_Water_A_Triply_Green_Synthesis/19074098

الاتاحة: https://doi.org/10.6084/m9.figshare.19074098.v1

المؤلفون: Majid Mommahed Heravi (9225485), Mansoureh Daraie (6995462)

مصطلحات موضوعية: Organic Chemistry, Nuclear Chemistry, Non-metal Chemistry, Nanochemistry and Supramolecular Chemistry, Optical Properties of Materials, Natural Products Chemistry, Organic Green Chemistry, Organic Chemistry not elsewhere classified, Quantum Chemistry, Organometallic Chemistry, Pyrazole, pyrido[2,3-d]pyrimidine-diones, green synthesis, four-component reaction

Relation: https://figshare.com/articles/journal_contribution/Molecular_diversity_of_four-component_synthesis_of_pyrazole-based_pyrido_2_3-d_pyrimidine-diones_in_water_a_green_synthesis/19074314

الاتاحة: https://doi.org/10.6084/m9.figshare.19074314.v1

المؤلفون: Fengru Zhou (8911442), Liwei Zhou (275029), Pengyang Jing (12054322), Mingjie Sun (4636345), Guobo Deng (5179793), Yun Liang (383275), Yuan Yang (151457)

مصطلحات موضوعية: Biochemistry, Cell Biology, Physiology, Biotechnology, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, c2 insertion units, 6 ­( 5, iodophenyl )- 2, heck /[ 4, different aryl iodides, aryl iodides, substrates enables, spiro polycycles, palladacycles formed, n <, iodo -<, interesting fused, h <, employing 2, cyclic β, chemoselectively act, chemoselective transformations, bromoacrylic acids, afford hexahydrodibenzoisoquinoline, access fused, >-( 2, >- methacryloylbenzamides, >)- diones

Relation: https://figshare.com/articles/journal_contribution/Chemoselective_Transformations_of_Cyclic_Bromoacrylic_Acids_with_Palladacycles_Formed_by_Aryl_Iodides_to_Access_Fused_or_Spiro_Polycycles/19131262

الاتاحة: https://doi.org/10.1021/acs.orglett.2c00254.s001

المؤلفون: Prior, Allan M, Gunaratna, Medha J, Kikuchi, Daisuke, Desper, John, Kim, Yunjeong, Chang, Kyeong-Ok, Maezawa, Izumi, Jin, Lee-Way, Hua, Duy H

المصدر: Synthesis. 46(16)

مصطلحات موضوعية: 3-substituted 7-methyl-2H-pyrano[3, 2-c]pyridine-2, 5(6H)-diones, dialkylation, fluorescence probes, heterocycles, tetra-hydro-1H, 9H-2, 10-dioxa-9-azaanthracen-1-ones, Analytical Chemistry, Organic Chemistry

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/25r1z367

المؤلفون: Milićević, David, Kimmel, Roman, Gazvoda, Martin, Urankar, Damijana, Kafka, Stanislav, Košmrlj, Janez

المصدر: Molecules, vol. 23, no. 9, art 2310, 2018. ; ISSN: 1420-3049

مصطلحات موضوعية: click chemistry, azido group, quinoline-2,4(1H,3H)-diones, propargyl group, bis(1,2,3-triazole), klik kemija, azido skupina, kinolin-2,4-(1H,3H)-dioni, propargilna skupina, bis(1,2,3-triazol), info:eu-repo/classification/udc/547.831.057

وصف الملف: application/pdf; text/url

Relation: info:eu-repo/grantAgreement/Drugi//IGA%2FFT%2F2018%2F007; info:eu-repo/grantAgreement/ARRS//P1-0230; info:eu-repo/grantAgreement/ARRS//J1-8147; info:eu-repo/grantAgreement/ARRS//J1-9166; https://repozitorij.uni-lj.si/IzpisGradiva.php?id=131643; https://repozitorij.uni-lj.si/Dokument.php?id=149026&dn=; https://repozitorij.uni-lj.si/Dokument.php?id=149025&dn=; https://plus.si.cobiss.net/opac7/bib/1537888707?lang=sl

الاتاحة: https://repozitorij.uni-lj.si/IzpisGradiva.php?id=131643
https://repozitorij.uni-lj.si/Dokument.php?id=149026&dn=
https://repozitorij.uni-lj.si/Dokument.php?id=149025&dn=
https://plus.si.cobiss.net/opac7/bib/1537888707?lang=sl

المؤلفون: Kafka, Stanislav, Hauke, Sylvia, Salčinović, Arjana, Soidinsalo, Otto, Urankar, Damijana, Košmrlj, Janez

المصدر: Molecules, vol. 16, no. 5, pp. 4070-4081, 2011. ; ISSN: 1420-3049

مصطلحات موضوعية: cycloaddition, azides, quinoline-2,4(1H,3H)-diones, terminal alkynes, 1,2,3-triazoles, organska kemija, sinteza, organske sinteze, kataliza, cikloadicija, heterociklične spojine, heterociklični sistemi, heterocikli, derivati kinolona, kinoloni, azidi, azidokinoloni, terminalni alkini, triazoli, baker, info:eu-repo/classification/udc/547.831.057:547.79:546.561

وصف الملف: application/pdf; text/url

Relation: info:eu-repo/grantAgreement/Drugi/Ministry of Education, Youth and Sports of the Czech Republic/MSM7088352101; info:eu-repo/grantAgreement/Drugi/Ministry of Education, Youth and Sports of the Czech Republic, Programme KONTAKT/9-06-3; info:eu-repo/grantAgreement/ARRS//P1-0230; info:eu-repo/grantAgreement/ARRS//BI-CZ%2F07-08-018; https://repozitorij.uni-lj.si/IzpisGradiva.php?id=129624; https://repozitorij.uni-lj.si/Dokument.php?id=146636&dn=; https://repozitorij.uni-lj.si/Dokument.php?id=146635&dn=; https://plus.si.cobiss.net/opac7/bib/35032581?lang=sl

الاتاحة: https://repozitorij.uni-lj.si/IzpisGradiva.php?id=129624
https://repozitorij.uni-lj.si/Dokument.php?id=146636&dn=
https://repozitorij.uni-lj.si/Dokument.php?id=146635&dn=
https://plus.si.cobiss.net/opac7/bib/35032581?lang=sl

المؤلفون: Andrey N. Komogortsev (6453074), Boris V. Lichitsky (6453077), Valeriya G. Melekhina (9682064), Darina I. Nasyrova (11553353), Constantine V. Milyutin (11553356)

مصطلحات موضوعية: Biochemistry, Medicine, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Information Systems not elsewhere classified, starting terarylenes aimed, hexatriene system containing, competitive process leading, biologically active alcohols, 7 ­( 3, 7 -<, various acids, substituted oxazol, side reactions, ray diffraction, preparative method, photoinduced 6π, investigated photoreaction, first time, distinctive feature, developed based, cyclization products, >]­ oxazole, >)- diones

Relation: https://figshare.com/articles/journal_contribution/Photoinduced_6_-Electrocyclization_of_a_1_3_5-Hexatriene_System_Containing_an_Allomaltol_Fragment/16799519

الاتاحة: https://doi.org/10.1021/acs.joc.1c01902.s002

المؤلفون: Yulya Victorivna Martynenko, Oleksii Mykolayovich Antypenko, Olexandr Anatolievich Brazhko, Irina Borisivna Labenska, Sergii Ivanovich Kovalenko

المصدر: Acta Chimica Slovenica, Vol 66, Iss 1, Pp 145-154 (2019)

مصطلحات موضوعية: (3Н-quinazoline-4-ylidene)hydrazides of N-carboxyalkyl-(aralkyl-aryl-)-isoindoline-1,3-diones, 2-([1,2,4]triazolo[1,5-c]quinazoline-2-yl-)alkyl-(alkaryl-, aryl-)-hydroisoindole-1,3(2H)-diones, directed search, physico-chemical properties, spectral featu, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://journals.matheo.si/index.php/ACSi/article/view/4731; https://doaj.org/toc/1318-0207; https://doaj.org/toc/1580-3155

URL الوصول: https://doaj.org/article/1e6abbb714294cad91c0f4dd0086cf2c

المؤلفون: Bocknack, Brian M., Wang, Long-Cheng, Krische, Michael J., Halpern, Jack

المصدر: Proceedings of the National Academy of Sciences of the United States of America, 2004 Apr . 101(15), 5421-5424.

URL الوصول: https://www.jstor.org/stable/3371634

المؤلفون: Sree, B. Satya^{1, 1}, Rao, A. Lakshmana², Babu, P. Swathanthra³, Kiran, K. Surya³, Vandana, K.³

المصدر: Indian Journal of Pharmacy and Pharmacology 4(3):130-133. 2017

المصدر: Environmental Health Perspectives, 1998 Mar 01. 106(3), 155-166.

URL الوصول: https://www.jstor.org/stable/3434317