المؤلفون: Mikołaj Sadowski, Karolina Kula

المصدر: Molecules, Vol 29, Iss 21, p 5066 (2024)

مصطلحات موضوعية: nitrodiene, azomethine ylide, cycloaddition, synthesis, spectral characteristics, MEDT, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1420-3049/29/21/5066; https://doaj.org/toc/1420-3049

URL الوصول: https://doaj.org/article/08a407ddfb884425918e1d5e0bb3d7eb

المؤلفون: Xiaofeng Zhang, Xiaoming Ma, Wei Zhang

المصدر: Beilstein Journal of Organic Chemistry, Vol 19, Iss 1, Pp 1677-1693 (2023)

مصطلحات موضوعية: [3 + 2] cycloaddition, decarboxylation, 1,3-dipolar, double cycloaddition, one-pot synthesis, multicomponent reaction, semi-stabilized azomethine ylide, Science, Organic chemistry, QD241-441

وصف الملف: electronic resource

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

URL الوصول: https://doaj.org/article/31424f45d7da486da274332d3b1e59d1

المؤلفون: Irina F. Zhurko, Sergey A. Dobrynin, Yurii I. Glazachev, Yuri V. Gatilov, Igor A. Kirilyuk

المصدر: Molecules, Vol 29, Iss 3, p 599 (2024)

مصطلحات موضوعية: three-component domino reaction, azomethine ylide, 1,3-dipolar cycloaddition, reduction-resistant nitroxide, EPR, Organic chemistry, QD241-441

Relation: https://www.mdpi.com/1420-3049/29/3/599; https://doaj.org/toc/1420-3049; https://doaj.org/article/8d1d6076335a4f739d5d798f9147e472

الاتاحة: https://doi.org/10.3390/molecules29030599
https://doaj.org/article/8d1d6076335a4f739d5d798f9147e472

المؤلفون: Ivana Antol, Petar Štrbac, Yasujiro Murata, Davor Margetić

المصدر: International Journal of Molecular Sciences, Vol 25, Iss 12, p 6524 (2024)

مصطلحات موضوعية: 1,3-dipolar cycloadditions, DFT calculations, isatine, azomethine ylide, reaction mechanism, Biology (General), QH301-705.5, Chemistry, QD1-999

Relation: https://www.mdpi.com/1422-0067/25/12/6524; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067; https://doaj.org/article/25bc19f8b3ee43509d3b42420f64aaf5

الاتاحة: https://doi.org/10.3390/ijms25126524
https://doaj.org/article/25bc19f8b3ee43509d3b42420f64aaf5

المؤلفون: Panda, Siva S., Aziz, Marian N., Stawinski, Jacek, Girgis, Adel S.

المصدر: Molecules. 28(2)

مصطلحات موضوعية: cycloaddition, azomethine ylide, pyrrolidine, spiro-compound

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-214219
https://doi.org/10.3390/molecules28020668

المؤلفون: Sobhi, Chafia, Merzoud, Lynda, Bouasla, Souad, Nacereddine, Abdelmalek Khorief, Morell, Christophe, Chermette, Henry

المساهمون: Laboratoire Physico-Chimie Des Surfaces Et Interfaces, Université du 20 Août1955, B.P 26 Skikda 21000, Algeria, Chemometrics and theoretical chemistry. - Chimiométrie et chimie théorique, Institut des Sciences Analytiques (ISA), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), ISA-Theoretical chemistry and A.I. - Chimie théorique et Intelligence artificielle, Université de Lyon

المصدر: ISSN: 0192-8651.

مصطلحات موضوعية: Azomethine ylide Nitroalkene [3 + 2] Cycloaddition Selectivity MEDT Mechanism DFT Calculations, Azomethine ylide, Nitroalkene, [3 + 2] Cycloaddition, Selectivity, MEDT, Mechanism, DFT Calculations, [CHIM]Chemical Sciences

Relation: hal-03932754; https://cnrs.hal.science/hal-03932754; https://cnrs.hal.science/hal-03932754/document; https://cnrs.hal.science/hal-03932754/file/Chafia_draft-8janvier2023bw.pdf

الاتاحة: https://cnrs.hal.science/hal-03932754
https://cnrs.hal.science/hal-03932754/document
https://cnrs.hal.science/hal-03932754/file/Chafia_draft-8janvier2023bw.pdf
https://doi.org/10.1002/jcc.27080

المؤلفون: Chermette, Henry, Sobhi, Chafia, Merzoud, Lynda, Bouasla, Souad, Nacereddine, Abdelmalek Khorief, Morell, Christophe

المساهمون: Chemometrics and theoretical chemistry. - Chimiométrie et chimie théorique, Institut des Sciences Analytiques (ISA), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), Laboratoire Physico-Chimie Des Surfaces Et Interfaces, Université du 20 Août1955, B.P 26 Skikda 21000, Algeria

المصدر: ISSN: 0192-8651.

مصطلحات موضوعية: Azomethine ylide Nitroalkene [3 + 2] Cycloaddition Selectivity MEDT Mechanism DFT Calculations, Azomethine ylide, Nitroalkene, [3 + 2] Cycloaddition, Selectivity, MEDT, Mechanism, DFT Calculations, [CHIM]Chemical Sciences

Relation: hal-03932754; https://cnrs.hal.science/hal-03932754; https://cnrs.hal.science/hal-03932754/document; https://cnrs.hal.science/hal-03932754/file/Chafia_draft-8janvier2023bw.pdf

الاتاحة: https://cnrs.hal.science/hal-03932754
https://cnrs.hal.science/hal-03932754/document
https://cnrs.hal.science/hal-03932754/file/Chafia_draft-8janvier2023bw.pdf

المؤلفون: Cristóbal, Christian, Corral, César, Carretero Gonzálvez, Juan Carlos, Ribagorda Lobera, María, Adrio Sevilla, Francisco Javier

المساهمون: UAM. Departamento de Química Orgánica

مصطلحات موضوعية: 5 Hydroxymethylfurfural, Azomethine Ylide, Copper, Iminoester, Phosphorus, Química

وصف الملف: application/pdf

Relation: Chemical Communications; https://doi.org/10.1039/d3cc00499f; Gobierno de España. PID2020-113059GB-C22; Comunidad de Madrid. B2017/BMD-3867/RENIM-CM; Chemical Communications 59.29 (2023): 4336-4339; 1359-7345 (print); 1364-548X (online); http://hdl.handle.net/10486/709507; 4336; 29; 4339; 59

الاتاحة: http://hdl.handle.net/10486/709507
https://doi.org/10.1039/d3cc00499f

المؤلفون: Richa Sharma, Lalit Yadav, Ali Adnan Nasim, Ravi Kant Yadav, Rui Hong Chen, Neha Kumari, Fan Ruiqi, Ashoke Sharon, Nawal Kishore Sahu, Sirish Kumar Ippagunta, Paolo Coghi, Vincent Kam Wai Wong, Sandeep Chaudhary

المصدر: Molecules ; Volume 28 ; Issue 18 ; Pages: 6503

مصطلحات موضوعية: anticancer, spirooxindole, [3+2] cycloaddition, azomethine ylide, microwave

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Medicinal Chemistry; https://dx.doi.org/10.3390/molecules28186503

الاتاحة: https://doi.org/10.3390/molecules28186503

المؤلفون: Guosheng Yang, Sicheng Li, Qiumi Wang, Huabao Chen, Chunping Yang, Zhongqiong Yin, Xu Song, Li Zhang, Cuifen Lu, Guizhou Yue

المصدر: Molecules; Volume 28; Issue 3; Pages: 1034

مصطلحات موضوعية: azomethine ylide, cycloaddition, Knoevenagel adduct, spiropyridazine oxoindole, synthesis

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Organic Chemistry; https://dx.doi.org/10.3390/molecules28031034

الاتاحة: https://doi.org/10.3390/molecules28031034

المؤلفون: Abdulrahman I. Almansour, Natarajan Arumugam, Raju Suresh Kumar

المصدر: Journal of King Saud University: Science, Vol 32, Iss 7, Pp 3059-3064 (2020)

مصطلحات موضوعية: Azomethine ylide, Spiroindenoquinoxalinone, Spiropyrrolidines, Benzylidene piperidone, Ionic liquids, Science (General), Q1-390

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S1018364720302524; https://doaj.org/toc/1018-3647

URL الوصول: https://doaj.org/article/a1f30abbb7a14326bea4c63bd772ac94

المؤلفون: Valeriia V. Sennikova, Alena V. Zalaltdinova, Yulia M. Sadykova, Ayrat R. Khamatgalimov, Almir S. Gazizov, Alexandra D. Voloshina, Anna P. Lyubina, Syumbelya K. Amerhanova, Julia K. Voronina, Elena A. Chugunova, Nurbol O. Appazov, Alexander R. Burilov, Michail A. Pudovik

المصدر: International Journal of Molecular Sciences; Volume 23; Issue 22; Pages: 14348

مصطلحات موضوعية: phosphacoumarin, azomethine ylide, cycloaddition, anti-cancer, cytotoxicity, quantum chemistry

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Molecular Pharmacology; https://dx.doi.org/10.3390/ijms232214348

الاتاحة: https://doi.org/10.3390/ijms232214348

المؤلفون: Luis R. Domingo, Mar Ríos-Gutiérrez, Assem Barakat

المصدر: Molecules; Volume 27; Issue 19; Pages: 6532

مصطلحات موضوعية: Molecular Electron Density Theory (MEDT), [3+2] cycloaddition (32CA), azomethine ylide (AY), spirooxindoles, ferrocene, triazole

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Inorganic Chemistry; https://dx.doi.org/10.3390/molecules27196532

الاتاحة: https://doi.org/10.3390/molecules27196532

المؤلفون: Hessa H. Al-Rasheed, Abdullah Mohammed Al-Majid, M. Ali, Matti Haukka, Sherif Ramadan, Saied M. Soliman, Ayman El-Faham, Luis R. Domingo, Assem Barakat

المصدر: Symmetry; Volume 14; Issue 10; Pages: 2071

مصطلحات موضوعية: asymmetric synthesis, spirooxindole, triazole, ferrocene, azomethine ylide, [3 + 2] cycloaddition reaction, MEDT study

وصف الملف: application/pdf

Relation: Chemistry and Symmetry/Asymmetry; https://dx.doi.org/10.3390/sym14102071

الاتاحة: https://doi.org/10.3390/sym14102071

المؤلفون: Stanislav V. Shmakov, Diana K. Latypova, Tatiana V. Shmakova, Artem A. Rubinshtein, Mark V. Chukin, Sergei G. Zhuravskii, Nickolay A. Knyazev, Alexander V. Stepakov, Michael M. Galagudza, Vitali M. Boitsov

المصدر: International Journal of Molecular Sciences; Volume 23; Issue 18; Pages: 10759

مصطلحات موضوعية: 3-azaspiro[bicyclo[3.1.0]hexane-2,5′-pyrimidines], alloxan-derived azomethine ylide, cyclopropenes, cancer cell lines (K-562, HeLa, Jurkat, CT26, Vero), antiproliferative activity, cell motility, morphological changes (cytoskeleton), cell cycle, cell death, in vitro and in vivo activity

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Biochemistry; https://dx.doi.org/10.3390/ijms231810759

الاتاحة: https://doi.org/10.3390/ijms231810759

المؤلفون: Mezna Saleh Altowyan, Saied M. Soliman, Matti Haukka, Nora Hamad Al-Shaalan, Aminah A. Alkharboush, Assem Barakat

المصدر: Molecules; Volume 27; Issue 13; Pages: 4095

مصطلحات موضوعية: spirooxindole, ferrocene, triazole, azomethine ylide, [3 + 2] cycloaddition (32CA) reaction

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Inorganic Chemistry; https://dx.doi.org/10.3390/molecules27134095

الاتاحة: https://doi.org/10.3390/molecules27134095

المؤلفون: Altowyan, Mezna Saleh, Soliman, Saied M., Haukka, Matti, Al-Shaalan, Nora Hamad, Alkharboush, Aminah A., Barakat, Assem

مصطلحات موضوعية: spirooxindole, imidazo[2,1-b]thiazole, azomethine ylide, [3+2] cycloaddition (32CA) reaction, kiteet, heterosykliset yhdisteet

وصف الملف: application/pdf; fulltext

Relation: Crystals; 12; CONVID_104035416

الاتاحة: http://urn.fi/URN:NBN:fi:jyu-202201311340

المؤلفون: Altowyan, Mezna Saleh, Soliman, Saied M., Haukka, Matti, Al-Shaalan, Nora H., Alkharboush, Aminah A., Barakat, Assem

مصطلحات موضوعية: pyrrolo[2,1-a]isoquinoline, azomethine ylide, [3 + 2] cycloaddition (32CA) reaction, stereoselective, DFT, Hirshfeld, typpiyhdisteet, röntgenkristallografia, tiheysfunktionaaliteoria, kemiallinen synteesi, heterosykliset yhdisteet

وصف الملف: application/pdf; fulltext

Relation: Crystals; 12; CONVID_104135575

الاتاحة: http://urn.fi/URN:NBN:fi:jyu-202202071405

المؤلفون: Al-Rasheed, Hessa H., Al-Majid, Abdullah Mohammed, Ali, M., Haukka, Matti, Ramadan, Sherif, Soliman, Saied M., El-Faham, Ayman, Domingo, Luis R., Barakat, Assem

مصطلحات موضوعية: asymmetric synthesis, spirooxindole, triazole, ferrocene, azomethine ylide, [3 + 2] cycloaddition reaction, MEDT study, kemiallinen synteesi, heterosykliset yhdisteet

وصف الملف: application/pdf; fulltext

Relation: Symmetry; 10; 14; CONVID_164378765

الاتاحة: http://urn.fi/URN:NBN:fi:jyu-202212145627

المؤلفون: Altowyan, Mezna Saleh, Soliman, Saied M., Haukka, Matti, Al-Shaalan, Nora Hamad, Alkharboush, Aminah A., Barakat, Assem

مصطلحات موضوعية: spirooxindole, ferrocene, triazole, azomethine ylide, [3 + 2] cycloaddition (32CA) reaction

وصف الملف: application/pdf; fulltext

Relation: Molecules; 13; 27; CONVID_148908418

الاتاحة: http://urn.fi/URN:NBN:fi:jyu-202212205763