المؤلفون: Muñoz Torres, Miguel Ángel, Martínez Lara, Fernando, Solas Luera, Marta, Suarez Pantiga, Samuel, Sanz Díez, Roberto

مصطلحات موضوعية: Carbolithiation, Gold, Homogeneous catalysis, Nitrogen heterocycles, Organolithiums, Química analítica, Chemistry, Analytic

وصف الملف: application/pdf

Relation: Advanced Synthesis & Catalysis. 2022, V. 364, n. 21, p. 3716-3724; https://doi.org/10.1002/adsc.202200824; info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-115789GB-C21/ES/ESTRATEGIAS SINTETICAS SOSTENIBLES PARA LA TRANSFORMACION DIRECTA DE NITROCOMPUESTOS Y DESARROLLO DE NUEVAS REACCIONES CATALIZADAS POR ORO/; info:eu-repo/grantAgreement/Junta de Castilla y León//BU049P20//Estrategias sintéticas sostenibles para la halogenación directa de nitrocompuestos y la preparación de electrolitos orgánicos para baterías de flujo redox/; info:eu-repo/grantAgreement/Fundación Bancaria Caixa d'Estalvis i Pensions de Barcelona//LCF%2FPR%2FPR18%2F51130007// Fluoración Directa de Nitrocompuestos y Sales de Heteroaril Fosfonio: Síntesis de Fluorocompuestos/FluNitroPhos/; http://hdl.handle.net/10259/7416

الاتاحة: http://hdl.handle.net/10259/7416
https://doi.org/10.1002/adsc.202200824

المؤلفون: Pantaleo Musci, Marco Colella, Angela Altomare, Giuseppe Romanazzi, Nadeem S. Sheikh, Leonardo Degennaro, Renzo Luisi

المصدر: Molecules; Volume 27; Issue 9; Pages: 2847

مصطلحات موضوعية: azetidines, organolithiums, nitrogen dynamics, heterocyclic chemistry, computational chemistry

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Organic Chemistry; https://dx.doi.org/10.3390/molecules27092847

الاتاحة: https://doi.org/10.3390/molecules27092847

المؤلفون: Tsybulin, Semyon V., Kaplanskiy, Mark V., Antonov, Alexander S.

مصطلحات موضوعية: organolithiums · indoles · heterocycles · nucleophilic substitution · naphthalene, 540 Chemie

Relation: http://doi.org/10.1002/chem.202303768; https://dx.doi.org/10.1002/chem.202303768

الاتاحة: https://dx.doi.org/10.5283/epub.55500
https://epub.uni-regensburg.de/id/eprint/55500

المؤلفون: Fournier, Anne

المساهمون: Clayden, Jonathan

مصطلحات موضوعية: 541.39, carbamates, organolithiums, arylation/vinylation, stereospecific, carbolithiation

URL الوصول: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.553501

المؤلفون: Musci, Pantaleo, von Keutz, Timo, Belaj, Ferdinand, Degennaro, Leonardo, Cantillo, David, Kappe, Oliver C, Luisi, Renzo

المساهمون: Musci, Pantaleo, von Keutz, Timo, Belaj, Ferdinand, Degennaro, Leonardo, Cantillo, David, Kappe, Oliver C, Luisi, Renzo

مصطلحات موضوعية: Flow Chemistry, Organolithiums, Strained Heterocycles, Azetidines, Azabicylo[1.1.0]butanes

Relation: info:eu-repo/semantics/altIdentifier/pmid/33325599; info:eu-repo/semantics/altIdentifier/wos/WOS:000617955600001; volume:60; firstpage:6395; lastpage:6399; numberofpages:5; journal:ANGEWANDTE CHEMIE. INTERNATIONAL EDITION; https://hdl.handle.net/11586/351068

الاتاحة: https://hdl.handle.net/11586/351068
https://doi.org/10.1002/anie.202014881

المؤلفون: Stent, Matthew A. H.

مصطلحات موضوعية: 547, Organolithiums

URL الوصول: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.249277

المؤلفون: Musci P., Colella M., Sivo A., Romanazzi G., Luisi R., Degennaro L.

المساهمون: Musci, P., Colella, M., Sivo, A., Romanazzi, G., Luisi, R., Degennaro, L.

مصطلحات موضوعية: Microreactor technology, carbenoid, organolithiums, chloroaldehydes

Relation: info:eu-repo/semantics/altIdentifier/pmid/32276538; info:eu-repo/semantics/altIdentifier/wos/WOS:000530076400063; volume:22; issue:9; firstpage:3623; lastpage:3627; numberofpages:5; journal:ORGANIC LETTERS; https://hdl.handle.net/11586/351066

الاتاحة: https://hdl.handle.net/11586/351066
https://doi.org/10.1021/acs.orglett.0c01085

المؤلفون: Yakubenko, Artyom A., Tupikina, Elena Yu., Antonov, Alexander S.

مصطلحات موضوعية: organolithiums · conjugation · coordination · regioselectivity · naphthalene, 540 Chemie

Relation: http://doi.org/10.1002/chem.202301439; https://dx.doi.org/10.1002/chem.202301439

الاتاحة: https://dx.doi.org/10.5283/epub.54521
https://epub.uni-regensburg.de/id/eprint/54521

المؤلفون: Marco Colella, Pantaleo Musci, Leonardo Degennaro, Renzo Luisi

المساهمون: Marco Colella, Pantaleo Musci, Leonardo Degennaro, Renzo Luisi, Colella, Marco, Musci, Pantaleo, Degennaro, Leonardo, Luisi, Renzo

مصطلحات موضوعية: reactive intermediates, organolithiums, flow chemistry, microreactor technology

Relation: ispartofbook:Book of Abstracts_13th Spanish-Italian Symposium on Organic Chemistry (SISOC XIII); 13th Spanish-Italian Symposium on Organic Chemistry (SISOC XIII); firstpage:OC-07; https://hdl.handle.net/11586/428784

الاتاحة: https://hdl.handle.net/11586/428784

المؤلفون: R. Luisi, L. Degennaro, M. Colella

المساهمون: Renzo Luisi, Leonardo Degennaro, Marco Colella, G. Parkin, K. Meyer, D. O’hare, Luisi, R., Degennaro, L., Colella, M.

مصطلحات موضوعية: Organolithiums, Alkyllithiums, Heterosubstituted organolithiums, Carbenoids, Carbanions, Stereoselectivity, Chemoselectivity, Catalysis, Cross-couplings, Directed Lithiation, Ring-strain, Flow Chemistry, Asymmetric Synthesis, Organic Synthesis

Relation: info:eu-repo/semantics/altIdentifier/isbn/9780124095472; ispartofbook:Reference Module in Chemistry, Molecular Sciences and Chemical Engineering; volume:11; firstpage:2; lastpage:56; numberofpages:55; alleditors:G. Parkin, K. Meyer, D. O’hare; https://hdl.handle.net/11586/428507; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85148667491; https://www.sciencedirect.com/science/article/abs/pii/B9780128202067000494?via=ihub

الاتاحة: https://hdl.handle.net/11586/428507
https://doi.org/10.1016/b978-0-12-820206-7.00049-4
https://www.sciencedirect.com/science/article/abs/pii/B9780128202067000494?via=ihub

المؤلفون: DILAURO, GIUSEPPE, DELL'AERA, MARZIA, VITALE, PAOLA, CAPRIATI, Vito, PERNA, FILIPPO

المساهمون: Dilauro, Giuseppe, Dell'Aera, Marzia, Vitale, Paola, Capriati, Vito, Perna, Filippo

مصطلحات موضوعية: Azo compounds, Grignard reagents, nucleophilic addition, organolithiums, water chemistry

Relation: info:eu-repo/semantics/altIdentifier/pmid/28695616; info:eu-repo/semantics/altIdentifier/wos/WOS:000407173600030; volume:56; issue:34; firstpage:10200; lastpage:10203; numberofpages:4; journal:ANGEWANDTE CHEMIE. INTERNATIONAL EDITION; http://hdl.handle.net/11586/197847; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85026896957

الاتاحة: http://hdl.handle.net/11586/197847
https://doi.org/10.1002/anie.201705412

المؤلفون: Parisi, Giovanna, COLELLA, MARCO, Monticelli, Serena, Romanazzi, Giuseppe, Holzer, Wolfgang, Langer, Thierry, Degennaro, Leonardo, Pace, Vittorio, Luisi, Renzo

المساهمون: Parisi, Giovanna, Colella, Marco, Monticelli, Serena, Romanazzi, Giuseppe, Holzer, Wolfgang, Langer, Thierry, Degennaro, Leonardo, Pace, Vittorio, Luisi, Renzo

مصطلحات موضوعية: Organolithiums, Fluorinated Molecules, Direct Fluoroalkylation, Synthesis

Relation: info:eu-repo/semantics/altIdentifier/pmid/28892363; info:eu-repo/semantics/altIdentifier/wos/WOS:000412716900016; volume:139; issue:39; firstpage:13648; lastpage:13651; numberofpages:4; journal:JOURNAL OF THE AMERICAN CHEMICAL SOCIETY; http://hdl.handle.net/11586/208237; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85032624588

الاتاحة: http://hdl.handle.net/11586/208237
https://doi.org/10.1021/jacs.7b07891

المؤلفون: Fabrice Burel, Rainier Hreiz, Aiichiro Nagaki, Daniela Vuluga, Julien Legros, Jean-Marc Commenge, Isabelle Chataigner, Katia Pérez, Jacques Maddaluno, Baptiste Picard, Jun-ichi Yoshida, Laurent Falk

المساهمون: Chimie Organique et Bioorganique : Réactivité et Analyse (COBRA), Institut Normand de Chimie Moléculaire Médicinale et Macromoléculaire (INC3M), Institut de Chimie du CNRS (INC)-École Nationale Supérieure d'Ingénieurs de Caen (ENSICAEN), Normandie Université (NU)-Normandie Université (NU)-Institut national des sciences appliquées Rouen Normandie (INSA Rouen Normandie), Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Université Le Havre Normandie (ULH), Normandie Université (NU)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Centre National de la Recherche Scientifique (CNRS)-Université de Caen Normandie (UNICAEN), Normandie Université (NU)-Institut de Chimie du CNRS (INC)-École Nationale Supérieure d'Ingénieurs de Caen (ENSICAEN), Normandie Université (NU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie Organique Fine (IRCOF), Université de Rouen Normandie (UNIROUEN), Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS), Polymères Biopolymères Surfaces (PBS), Institut national des sciences appliquées Rouen Normandie (INSA Rouen Normandie), Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Institut de Chimie du CNRS (INC)-Institut Normand de Chimie Moléculaire Médicinale et Macromoléculaire (INC3M), Normandie Université (NU)-École Nationale Supérieure d'Ingénieurs de Caen (ENSICAEN), Normandie Université (NU)-Université Le Havre Normandie (ULH), Normandie Université (NU)-Centre National de la Recherche Scientifique (CNRS), Laboratoire Réactions et Génie des Procédés (LRGP), Centre National de la Recherche Scientifique (CNRS)-Université de Lorraine (UL), Kyoto University [Kyoto], National Institute of Technology (KOSEN), Laboratoire de chimie théorique (LCT), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Institut de Chimie Organique Fine (IRCOF), Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Centre National de la Recherche Scientifique (CNRS)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)-Institut Normand de Chimie Moléculaire Médicinale et Macromoléculaire (INC3M), Université de Caen Normandie (UNICAEN), Normandie Université (NU)-Normandie Université (NU)-Centre National de la Recherche Scientifique (CNRS)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Institut national des sciences appliquées Rouen Normandie (INSA Rouen Normandie), Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-École Nationale Supérieure d'Ingénieurs de Caen (ENSICAEN), Normandie Université (NU)-Université de Caen Normandie (UNICAEN), Normandie Université (NU)-Centre National de la Recherche Scientifique (CNRS)-Université Le Havre Normandie (ULH), Normandie Université (NU), Centre National de la Recherche Scientifique (CNRS)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Institut Normand de Chimie Moléculaire Médicinale et Macromoléculaire (INC3M), Université de Lorraine (UL)-Centre National de la Recherche Scientifique (CNRS), Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)

المصدر: Organic Process Research and Development
Organic Process Research and Development, American Chemical Society, 2020, 24 (5), pp.787-791. ⟨10.1021/acs.oprd.0c00203⟩

مصطلحات موضوعية: Materials science, Proton, microflow, Analytical chemistry, chemistry.chemical_element, carbenoid, stereoselectivity, 010402 general chemistry, 01 natural sciences, 7. Clean energy, [CHIM.GENI]Chemical Sciences/Chemical engineering, [CHIM]Chemical Sciences, Physical and Theoretical Chemistry, Bromine, organolithium, [CHIM.ORGA]Chemical Sciences/Organic chemistry, 010405 organic chemistry, Organic Chemistry, Organolithiums, Microreactor design, 0104 chemical sciences, Volumetric flow rate, chemistry, Yield (chemistry), Electrophile, Stereoselectivity, Lithium, Selectivity, microreactor shape

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5881e23b94691bbcb2f101491d4fcef3
https://doi.org/10.1021/acs.oprd.0c00203

المؤلفون: Aiichiro Nagaki, Yuki Uesugi, Yutaka Tomida, Jun-ichi Yoshida

المصدر: Beilstein Journal of Organic Chemistry, Vol 7, Iss 1, Pp 1064-1069 (2011)

مصطلحات موضوعية: homocoupling, iron salts, microreactor, organolithiums, Science, Organic chemistry, QD241-441

وصف الملف: electronic resource

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

URL الوصول: https://doaj.org/article/012b95c689914580a26aa962ce1e9059

المؤلفون: Musci P., Colella M., Andresini M., Aramini A., Degennaro L., Luisi R.

المساهمون: Musci, P., Colella, M., Andresini, M., Aramini, A., Degennaro, L., Luisi, R.

مصطلحات موضوعية: 1-azabicyclo[1.1.0]butanes, flow technology, strained heterocycles, organolithiums

Relation: info:eu-repo/semantics/altIdentifier/pmid/35536561; info:eu-repo/semantics/altIdentifier/wos/WOS:000792841600001; volume:58; issue:43; firstpage:6356; lastpage:6359; numberofpages:4; journal:CHEMICAL COMMUNICATIONS; https://hdl.handle.net/11586/428506; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85131107769; https://www.rsc.org/journals-books-databases/about-journals/chemcomm/

الاتاحة: https://hdl.handle.net/11586/428506
https://doi.org/10.1039/d2cc01641a
https://www.rsc.org/journals-books-databases/about-journals/chemcomm/

المؤلفون: Sassone F. C, PERNA, FILIPPO, Salomone A, Florio S, CAPRIATI, Vito

المساهمون: Sassone, F. C., Perna, Filippo, Salomone, A, Florio, S, Capriati, Vito

مصطلحات موضوعية: Lateral lithiation, organolithiums, tetrahydrofurans, deep eutectic solvents

Relation: info:eu-repo/semantics/altIdentifier/pmid/25959580; info:eu-repo/semantics/altIdentifier/wos/WOS:000355345700009; volume:51; firstpage:9459; lastpage:9462; numberofpages:4; journal:CHEMICAL COMMUNICATIONS; http://hdl.handle.net/11586/139581; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84930226139

الاتاحة: http://hdl.handle.net/11586/139581
https://doi.org/10.1039/c5cc02884a

المؤلفون: DEGENNARO, LEONARDO, Flavio Fanelli, Arianna Giovine, LUISI, Renzo

المساهمون: Degennaro, Leonardo, Flavio, Fanelli, Arianna, Giovine, Luisi, Renzo

مصطلحات موضوعية: carbenoids - flow chemistry - microreactor technology - organolithiums - sustainable chemistry

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000347705400002; volume:357; issue:1; firstpage:21; lastpage:27; numberofpages:7; journal:ADVANCED SYNTHESIS & CATALYSIS; http://hdl.handle.net/11586/37934; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84920733710

الاتاحة: http://hdl.handle.net/11586/37934
https://doi.org/10.1002/adsc.201400747
http://onlinelibrary.wiley.com/doi/10.1002/adsc.201400747/abstract

المؤلفون: Nishimura, Katsumi, Fukuyama, Naoshi, Yasuhara, Tomohisa, Yamashita, Mitsuaki, Sumiyoshi, Takaaki, Yamamoto, Yasutomo, Yamada, Ken-ichi, Tomioka, Kiyoshi

المساهمون: 山田, 健一, 富岡, 清

مصطلحات موضوعية: Chiral ligand, Asymmetric synthesis, Organolithiums, Conjugate addition, Lycorane

وصف الملف: application/pdf

Relation: http://hdl.handle.net/2433/201854; AA00861787; Tetrahedron; 71; 39; 7222; 7226

الاتاحة: http://hdl.handle.net/2433/201854

المؤلفون: Ghinato S., Territo D., Maranzana A., Capriati V., Blangetti M., Prandi C.

المساهمون: Ghinato, S., Territo, D., Maranzana, A., Capriati, V., Blangetti, M., Prandi, C.

مصطلحات موضوعية: amides, carbanions, chemoselectivity, ketones, organolithiums

Relation: info:eu-repo/semantics/altIdentifier/pmid/33150980; info:eu-repo/semantics/altIdentifier/wos/WOS:000607583600001; volume:27; issue:8; firstpage:2868; lastpage:2874; numberofpages:7; journal:CHEMISTRY-A EUROPEAN JOURNAL; http://hdl.handle.net/11586/359393; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85099472021

الاتاحة: http://hdl.handle.net/11586/359393
https://doi.org/10.1002/chem.202004840

المؤلفون: Marco Blangetti, Cristina Prandi, Davide Territo, Vito Capriati, Andrea Maranzana, Simone Ghinato

مصطلحات موضوعية: Time Factors, ketones, Carboxylic acid, Cyclopentyl methyl ether, 010402 general chemistry, 01 natural sciences, Catalysis, chemistry.chemical_compound, carbanions, amides, chemoselectivity, organolithiums, Amides, Density Functional Theory, Ketones, Lithium Compounds, Air, Reactivity (chemistry), Chemoselectivity, Carbanion, chemistry.chemical_classification, 010405 organic chemistry, Organic Chemistry, Nucleophilic acyl substitution, General Chemistry, Combinatorial chemistry, 0104 chemical sciences, chemistry, Reagent, Yield (chemistry)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84f06c001ceb7bf7f76368966181908c
http://hdl.handle.net/2318/1788723