المؤلفون: Pradnya Patil, Nisha Nerlekar, Sanket Rathod, Pradeep Mhaldar, Taha Najm, Prakash Bansode, Jagannath Jadhav, Padma Dandge, Prafulla Choudhari, Dattaprasad Pore, Gajanan Rashinkar

المصدر: Results in Chemistry, Vol 7, Iss , Pp 101476- (2024)

مصطلحات موضوعية: Sulphonamide-azaheterocycle conjugates, Anti-cancer, DAPI, Anti-inflammatory, Anti-diabetic activity, Antiangiogenic activity, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2211715624001723; https://doaj.org/toc/2211-7156

URL الوصول: https://doaj.org/article/cd70cd4ccf05483981e749756abb36b9

المؤلفون: Cozzi, Pier Giorgio, Calogero, Francesco, Wilczek, Leonie, Pinosa, Emanuele, Gualandi, Andrea, Dorta, Romano, Herrera, Alberto, Dai, Yasi, Rossignol, Arthur, Negri, Fabrizia, Ziani, Zakaria, Fermi, Andrea, Ceroni, Paola

المساهمون: Cozzi, Pier Giorgio, Calogero, Francesco, Wilczek, Leonie, Pinosa, Emanuele, Gualandi, Andrea, Dorta, Romano, Herrera, Alberto, Dai, Yasi, Rossignol, Arthur, Negri, Fabrizia, Ziani, Zakaria, Fermi, Andrea, Ceroni, Paola

مصطلحات موضوعية: Azaheterocycle, Meisenheimer adduct, Photoreductant, Reduction, nBuLi

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/pmid/39078744; info:eu-repo/semantics/altIdentifier/wos/WOS:001342073200007; volume:63; issue:144; firstpage:1; lastpage:12; numberofpages:12; journal:ANGEWANDTE CHEMIE. INTERNATIONAL EDITION; https://hdl.handle.net/11585/985574

الاتاحة: https://hdl.handle.net/11585/985574
https://doi.org/10.1002/anie.202411074
https://onlinelibrary.wiley.com/doi/10.1002/anie.202411074

المؤلفون: GABRIELE MICHELETTI, Boga Carla, Giacomo Drius, silvia bordoni, Natalia Calonghi

المساهمون: GABRIELE MICHELETTI, Boga Carla, Giacomo Driu, silvia bordoni, Natalia Calonghi

مصطلحات موضوعية: HDAC, SAHA, anticancer, azaheterocycle, synthesis

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/pmid/38202821; info:eu-repo/semantics/altIdentifier/wos/WOS:001140442400001; volume:29; issue:1; firstpage:1; lastpage:23; numberofpages:23; journal:MOLECULES; https://hdl.handle.net/11585/955188; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85181970592; https://www.mdpi.com/1420-3049/29/1/238

الاتاحة: https://hdl.handle.net/11585/955188
https://doi.org/10.3390/molecules29010238
https://www.mdpi.com/1420-3049/29/1/238

المؤلفون: Elena Y. Mendogralo, Larisa Y. Nesterova, Ekaterina R. Nasibullina, Roman O. Shcherbakov, Alexander G. Tkachenko, Roman Y. Sidorov, Maxim A. Sukonnikov, Dmitry A. Skvortsov, Maxim G. Uchuskin

المصدر: Molecules, Vol 28, Iss 14, p 5348 (2023)

مصطلحات موضوعية: azaheterocycle, indole, quinazolinone, antibacterial activity, resistance, Mycobacterium smegmatis, Organic chemistry, QD241-441

Relation: https://www.mdpi.com/1420-3049/28/14/5348; https://doaj.org/toc/1420-3049; https://doaj.org/article/2342e8a5d93046d29a2afdb4733ad8dc

الاتاحة: https://doi.org/10.3390/molecules28145348
https://doaj.org/article/2342e8a5d93046d29a2afdb4733ad8dc

المؤلفون: Elena Y. Mendogralo, Larisa Y. Nesterova, Ekaterina R. Nasibullina, Roman O. Shcherbakov, Danil A. Myasnikov, Alexander G. Tkachenko, Roman Y. Sidorov, Maxim G. Uchuskin

المصدر: Molecules, Vol 28, Iss 7095, p 7095 (2023)

مصطلحات موضوعية: azaheterocycle, indole, antibacterial activity, resistance, molecular docking, Organic chemistry, QD241-441

Relation: https://www.mdpi.com/1420-3049/28/20/7095; https://doaj.org/toc/1420-3049; https://doaj.org/article/e9899a5e251248f7952fc4afcdc4ac35

الاتاحة: https://doi.org/10.3390/molecules28207095
https://doaj.org/article/e9899a5e251248f7952fc4afcdc4ac35

المؤلفون: Goya, Tsuyoshi, Crocomo, Paola Zimmermann, Hosono, Takumi, Minakata, Satoshi, de Sousa, Leonardo Evaristo, de Silva, Piotr, Data, Przemyslaw, Takeda, Youhei

المصدر: Goya , T , Crocomo , P Z , Hosono , T , Minakata , S , de Sousa , L E , de Silva , P , Data , P & Takeda , Y 2022 , ' A New Entry to Purely Organic Thermally Activated Delayed Fluorescence Emitters Based on Pyrido[2,3‐ b ]pyrazine–Dihydrophenazasilines Donor–Acceptor Dyad ' , Asian Journal of Organic Chemistry , vol. 11 , no. 3 , e202100780 . https://doi.org/10.1002/ajoc.202100780

مصطلحات موضوعية: Thermally activated delayed fluorescence, Donor-acceptor, Charge-transfer, OLED, Azaheterocycle

وصف الملف: application/pdf

Relation: https://orbit.dtu.dk/en/publications/9a4926d7-6a1a-427b-bc8e-31dcffdbcd73

الاتاحة: https://orbit.dtu.dk/en/publications/9a4926d7-6a1a-427b-bc8e-31dcffdbcd73
https://doi.org/10.1002/ajoc.202100780
https://backend.orbit.dtu.dk/ws/files/282772470/Asian_J_Org_Chem_2022_Goya_A_New_Entry_to_Purely_Organic_Thermally_Activated_Delayed_Fluorescence_Emitters_Based_on.pdf

المؤلفون: Kun Hu (119408), Ruiting Liu (2168947), Xigeng Zhou (1701397)

مصطلحات موضوعية: Biophysics, Biochemistry, Genetics, Molecular Biology, Biotechnology, Evolutionary Biology, Developmental Biology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, reaction conditions, additive, Such transformations, dibenzo, intramolecular, seven-membered azaheterocycle, selectivity, amines, Multiple, access, Nitrile, atom-economy, material, Sequential Addition, azepine, 2-, Bond, earth metal-catalyzed sequential, construction, Amine, Amino

Relation: https://figshare.com/articles/journal_contribution/Sequential_Addition_of_Amines_to_Nitrile_and_Carbon_Carbon_Multiple_Bond_A_Route_to_7_Amino_5_i_H_i_dibenzo_i_c_e_i_azepines/15831757

الاتاحة: https://doi.org/10.1021/acs.orglett.1c02540.s001

المؤلفون: Sehan Lee, Mace G. Barron

المصدر: Journal of Cheminformatics, Vol 10, Iss 1, Pp 1-13 (2018)

مصطلحات موضوعية: Aromatase inhibitor, Adverse outcome pathway, 3D-QSAR, Steroid, Azaheterocycle, Hydrophobic contact, Information technology, T58.5-58.64, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s13321-017-0253-8; https://doaj.org/toc/1758-2946

URL الوصول: https://doaj.org/article/11de3ba0488b4fb5844eac4a08cd9866

المؤلفون: Le Guen, Clothilde, Mazzah, Ahmed, Penhoat, Maël, Melnyk, Patricia, Rolando, Christian, Chausset-Boissarie, Laetitia

المساهمون: Miniaturisation pour la Synthèse, l’Analyse et la Protéomique - UAR 3290 (MSAP), Institut de Chimie - CNRS Chimie (INC-CNRS)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Lille Neurosciences & Cognition - U 1172 (LilNCog), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille)

المصدر: ISSN: 0039-7881 ; EISSN: 1437-210X.

مصطلحات موضوعية: Fluorination, azaheterocycle, Selectfluor, 2-methylpyridines, 2-methylquinolines, [CHIM.ORGA]Chemical Sciences/Organic chemistry, [CHIM.THER]Chemical Sciences/Medicinal Chemistry

Relation: hal-03061701; https://hal.science/hal-03061701; https://hal.science/hal-03061701/document; https://hal.science/hal-03061701/file/Direct%20and%20regioselective%20C%28sp3%29-H%20bond%20fluorination%20of%202-alkyl%20azaarenes%20with%20selectfluor.pdf

الاتاحة: https://hal.science/hal-03061701
https://hal.science/hal-03061701/document
https://hal.science/hal-03061701/file/Direct%20and%20regioselective%20C%28sp3%29-H%20bond%20fluorination%20of%202-alkyl%20azaarenes%20with%20selectfluor.pdf
https://doi.org/10.1055/s-0040-1706482

المؤلفون: Perekhoda, L

المصدر: Annals of Mechnikov's Institute; № 4 (2014); 55-60

مصطلحات موضوعية: Pharmacy, docking, anticonvulsant activity, PASS computer program, di (three) azaheterocycle

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=scientific_p::065bd150207412c7dab180e0b3395c0c
http://journals.uran.ua/ami/article/view/208223

المؤلفون: A. Khalafi-nezhada, A. Zareb, A. Parhamia, A. Hasaninejadc, A. R. Moosavi Zarea

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://www.sid.ir/En/VEWSSID/J_pdf/8832008S304.pdf.

مصطلحات موضوعية: Quaternary ammonium salt, N-Alkylation, Azaheterocycle, Microwave, Green chemistry

وصف الملف: application/pdf

Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.544.582; http://www.sid.ir/En/VEWSSID/J_pdf/8832008S304.pdf

الاتاحة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.544.582
http://www.sid.ir/En/VEWSSID/J_pdf/8832008S304.pdf

المؤلفون: Chausset-Boissarie, Laetitia, Le Guen, Clothilde, Mazzah, Ahmed, PENHOAT, Maël, Melnyk, Patricia, Rolando, Christian

المساهمون: CHU Lille, Inserm, Université de Lille, 462133, Lille Neurosciences & Cognition (LilNCog) - U 1172

مصطلحات موضوعية: fluorination, 2-methylquinolines, 2-methylpyridines, Selectfluor, azaheterocycle

Relation: Synthesis; http://hdl.handle.net/20.500.12210/40315

الاتاحة: https://hdl.handle.net/20.500.12210/40315

المؤلفون: Ouchakour, Lamiaa, Nonn, Melinda, D'hooghe, Matthias, Kiss, Lorand

المصدر: JOURNAL OF FLUORINE CHEMISTRY ; ISSN: 0022-1139 ; ISSN: 1873-3328

مصطلحات موضوعية: Chemistry, RING-EXPANSION, FACILE SYNTHESIS, PIPERIDINE, ACIDS, Benzazepine, Fluorine, Reductive amination, Ring expansion, Azaheterocycle, Ring closing

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

Relation: https://biblio.ugent.be/publication/8691845; http://hdl.handle.net/1854/LU-8691845; http://dx.doi.org/10.1016/j.jfluchem.2020.109466; https://biblio.ugent.be/publication/8691845/file/8691846

الاتاحة: https://biblio.ugent.be/publication/8691845
http://hdl.handle.net/1854/LU-8691845
https://doi.org/10.1016/j.jfluchem.2020.109466
https://biblio.ugent.be/publication/8691845/file/8691846

المؤلفون: Clothilde Le Guen, Patricia Melnyk, Christian Rolando, Laëtitia Chausset-Boissarie, Ahmed Mazzah, Maël Penhoat

المساهمون: Miniaturisation pour la Synthèse, l’Analyse et la Protéomique - UAR 3290 (MSAP), Université de Lille-Centre National de la Recherche Scientifique (CNRS), Lille Neurosciences & Cognition - U 1172 (LilNCog), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Miniaturisation pour la Synthèse, l’Analyse et la Protéomique - USR 3290 (MSAP), Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Lille Neurosciences & Cognition - U 1172 (LilNCog (ex-JPARC)), Chausset-Boissarie, laetitia

المصدر: Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, 2020, 53 (6), pp.1157-1162. ⟨10.1055/s-0040-1706482⟩
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2020, 53 (6), pp.1157-1162. ⟨10.1055/s-0040-1706482⟩

مصطلحات موضوعية: 0303 health sciences, 010405 organic chemistry, Chemistry, Hydrogen bond, 2-methylpyridines, [CHIM.ORGA]Chemical Sciences/Organic chemistry, [CHIM.THER] Chemical Sciences/Medicinal Chemistry, Organic Chemistry, Regioselectivity, 2-methylquinolines, [CHIM.THER]Chemical Sciences/Medicinal Chemistry, [CHIM.ORGA] Chemical Sciences/Organic chemistry, 01 natural sciences, Medicinal chemistry, Catalysis, 0104 chemical sciences, azaheterocycle, 03 medical and health sciences, chemistry.chemical_compound, Transition metal, Fluorination, Selectfluor, 030304 developmental biology

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35c214efd27d814864ff0ae188c2754b
https://hal.science/hal-03061701

المؤلفون: Ciccolini, Cecilia

المساهمون: Favi, Gianfranco, Ciccolini, Cecilia

مصطلحات موضوعية: Heterocycle, Azoalkene, Nucleophilic addition, CDC, Indole, Green- chemistry, Indoline, Regioselectivity, Umpolung α-(hetero)arylation, Michael addition, Metal and oxidant free, Benzofuran, Polycyclic indoline, Divergent synthesi, [3+2]/[4+2] Annulation, Indole-pyrazol-5-one, Indole-pyridazine, Synthon, Poly-azaheterocycle, Multicomponent reaction, 1-Amino-1H- imidazole-2(3H)-thione derivative, α-Halohydrazones

Relation: numberofpages:194; alleditors:Favi, Gianfranco; http://hdl.handle.net/11576/2674162

الاتاحة: http://hdl.handle.net/11576/2674162

المؤلفون: khodaei, mohammad mehdi

المساهمون: Razi University

المصدر: Indian Journal of Chemistry -Section A (IJCA); Vol 58, No 12 (2019): INDIAN JOURNAL OF CHEMISTRY- SECTION A; 1311-1318

مصطلحات موضوعية: theoretical chemistry, structure properties calculations, DFT calculations, Fused pyrrole, Electrophilicity, Energy gap, Azaheterocycle, Global descriptor

وصف الملف: application/pdf

Relation: http://op.niscair.res.in/index.php/IJCA/article/download/24014/465475079; http://op.niscair.res.in/index.php/IJCA/article/download/24014/465475080; http://op.niscair.res.in/index.php/IJCA/article/download/24014/465475081; http://op.niscair.res.in/index.php/IJCA/article/download/24014/465475082; http://op.niscair.res.in/index.php/IJCA/article/download/24014/465475083; http://op.niscair.res.in/index.php/IJCA/article/download/24014/465475084; http://op.niscair.res.in/index.php/IJCA/article/view/24014

الاتاحة: http://op.niscair.res.in/index.php/IJCA/article/view/24014

المؤلفون: Perekhoda L.O.

المصدر: Anali Mečnikìvsʹkogo Institutu, Vol 4, Pp 55-60 (2014)

مصطلحات موضوعية: lcsh:R5-920, PASS computer program, docking, anticonvulsant activity, di (three) azaheterocycle, lcsh:Medicine (General)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doajarticles::32531ca6e691e9d437f8e6d83ef26026
http://irbis-nbuv.gov.ua/cgi-bin/irbis_nbuv/cgiirbis_64.exe?C21COM=2&I21DBN=UJRN&P21DBN=UJRN&IMAGE_FILE_DOWNLOAD=1&Image_file_name=PDF/ami_2014_4_9.pdf

المؤلفون: Goya, Tsuyoshi, Crocomo, Paola Zimmermann, Hosono, Takumi, Minakata, Satoshi, de Sousa, Leonardo Evaristo, de Silva, Piotr, Data, Przemyslaw, Takeda, Youhei

المصدر: Goya , T , Crocomo , P Z , Hosono , T , Minakata , S , de Sousa , L E , de Silva , P , Data , P & Takeda , Y 2022 , ' A New Entry to Purely Organic Thermally Activated Delayed Fluorescence Emitters Based on Pyrido[2,3‐ b ]pyrazine–Dihydrophenazasilines Donor–Acceptor Dyad ' , Asian Journal of Organic Chemistry , vol. 11 , no. 3 , e202100780 .

مصطلحات الفهرس: Thermally activated delayed fluorescence, Donor-acceptor, Charge-transfer, OLED, Azaheterocycle, article

URL: https://orbit.dtu.dk/en/publications/9a4926d7-6a1a-427b-bc8e-31dcffdbcd73
https://doi.org/10.1002/ajoc.202100780
https://backend.orbit.dtu.dk/ws/files/282772470/Asian_J_Org_Chem_2022_Goya_A_New_Entry_to_Purely_Organic_Thermally_Activated_Delayed_Fluorescence_Emitters_Based_on.pdf