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Tytuł :
Visible-Light-Induced Organophotocatalytic Difunctionallization: Open-Air Hydroxysulfurization of Aryl Alkenes with Aryl Thiols.
Autorzy :
Hong JE; College of Pharmacy, Inje Institute of Pharmaceutical Sciences and Research, Inje University, 197 Inje-ro, Gimhae, Gyeongnam 50834, Republic of Korea.
Jung Y; College of Pharmacy, Inje Institute of Pharmaceutical Sciences and Research, Inje University, 197 Inje-ro, Gimhae, Gyeongnam 50834, Republic of Korea.
Min D; College of Pharmacy, Inje Institute of Pharmaceutical Sciences and Research, Inje University, 197 Inje-ro, Gimhae, Gyeongnam 50834, Republic of Korea.
Jang M; College of Pharmacy, Inje Institute of Pharmaceutical Sciences and Research, Inje University, 197 Inje-ro, Gimhae, Gyeongnam 50834, Republic of Korea.
Kim S; College of Pharmacy, Inje Institute of Pharmaceutical Sciences and Research, Inje University, 197 Inje-ro, Gimhae, Gyeongnam 50834, Republic of Korea.
Park J; Center for Catalytic Hydrocarbon Functionalizations, Institute for Basic Science (IBS) and Department of Chemistry, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of Korea.
Park Y; College of Pharmacy, Inje Institute of Pharmaceutical Sciences and Research, Inje University, 197 Inje-ro, Gimhae, Gyeongnam 50834, Republic of Korea.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 13. Date of Electronic Publication: 2022 May 13.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Organophotoredox-Catalyzed Reductive Tetrafluoroalkylation of Alkenes.
Autorzy :
Kostromitin VS; N. D. Zelinsky Institute of Organic Chemistry, Leninsky prosp. 47, 119991 Moscow, Russian Federation.; Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1-3, 119991 Moscow, Russian Federation.
Levin VV; N. D. Zelinsky Institute of Organic Chemistry, Leninsky prosp. 47, 119991 Moscow, Russian Federation.
Dilman AD; N. D. Zelinsky Institute of Organic Chemistry, Leninsky prosp. 47, 119991 Moscow, Russian Federation.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 13. Date of Electronic Publication: 2022 May 13.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Glycosyl o -[1-( p -MeO-Phenyl)vinyl]benzoates (PMPVB) as Easily Accessible, Stable, and Reactive Glycosyl Donors for O-, S-, and C-Glycosylations under Brønsted Acid Catalysis.
Autorzy :
Halder S; Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati, Assam 781039, India.
Addanki RB; Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati, Assam 781039, India.
Moktan S; Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati, Assam 781039, India.
Kancharla PK; Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati, Assam 781039, India.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 13. Date of Electronic Publication: 2022 May 13.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Synthesis of N -Substituted 1,2-Diazetidin-3-ones by the Ugi Reaction Comprising Chiral α-Hydrazino Acids.
Autorzy :
Suć Sajko J; Division of Organic Chemistry and Biochemistry, Ruđer Bošković Institute, Bijenička cesta 54, 10000 Zagreb, Croatia.
Jerić I; Division of Organic Chemistry and Biochemistry, Ruđer Bošković Institute, Bijenička cesta 54, 10000 Zagreb, Croatia.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 13. Date of Electronic Publication: 2022 May 13.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Synthesis of Aza[ n ]helicenes ( n = 4-7) via Photocyclodehydrochlorination of 1-Chloro- N -aryl-2-naphthamides.
Autorzy :
Váňa L
Jakubec M
Sýkora J
Císařová I; Department of Inorganic Chemistry, Faculty of Science, Charles University in Prague, Hlavova 2030, 128 40 Prague 2, Czech Republic.
Žádný J
Storch J
Církva V
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 12. Date of Electronic Publication: 2022 May 12.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Regioselective Access to 2-Iminoimidazolidines via AgF-Mediated Cascade Reactions.
Autorzy :
He Y; Artemisinin Research Center & The First Affiliated Hospital, Guangzhou University of Chinese Medicine, 12 Jichang Road, Guangzhou 510405, China.
Wu H; Artemisinin Research Center & The First Affiliated Hospital, Guangzhou University of Chinese Medicine, 12 Jichang Road, Guangzhou 510405, China.
Liang Y; Artemisinin Research Center & The First Affiliated Hospital, Guangzhou University of Chinese Medicine, 12 Jichang Road, Guangzhou 510405, China.
Deng H; Artemisinin Research Center & The First Affiliated Hospital, Guangzhou University of Chinese Medicine, 12 Jichang Road, Guangzhou 510405, China.
Xiang L; Artemisinin Research Center & The First Affiliated Hospital, Guangzhou University of Chinese Medicine, 12 Jichang Road, Guangzhou 510405, China.
Gu J; Research Centre for Integrative Medicine, School of Basic Medical Science, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Zhang J; Artemisinin Research Center & The First Affiliated Hospital, Guangzhou University of Chinese Medicine, 12 Jichang Road, Guangzhou 510405, China.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 12. Date of Electronic Publication: 2022 May 12.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Telescoped Oxidation and Cycloaddition of Urazoles to Access Diazacyclobutenes.
Autorzy :
Miller BA; Department of Chemistry, Clemson University, Clemson, South Carolina 29631, United States.
Narangoda CJ; Department of Chemistry, Faculty of Applied Sciences, University of Sri Jayewardenepura, Gangodawila, Nugegoda-10250, Sri Lanka.
Johnson TL; School of Medicine-Greenville, University of South Carolina, Greenville, South Carolina 29605, United States.
Barata RD; Department of Chemistry, Clemson University, Clemson, South Carolina 29631, United States.
Belue F; Department of Chemistry, Clemson University, Clemson, South Carolina 29631, United States.
Solomon EE; Department of Chemistry, Clemson University, Clemson, South Carolina 29631, United States.
Bragg AA; Department of Chemistry, Clemson University, Clemson, South Carolina 29631, United States.
Whitehead DC; Department of Chemistry, Clemson University, Clemson, South Carolina 29631, United States.; Eukaryotic Pathogens Innovation Center, Clemson University, Clemson, South Carolina 29634, United States.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 12. Date of Electronic Publication: 2022 May 12.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Polynitro- N -aryl-C-nitro-pyrazole/imidazole Derivatives: Thermally Stable-Insensitive Energetic Materials.
Autorzy :
Vangara S; School of Chemistry, University of Hyderabad, Hyderabad 500046, India.; Advanced Centre of Research in High Energy Materials, University of Hyderabad, Hyderabad 500046, India.
Kommu N; Advanced Centre of Research in High Energy Materials, University of Hyderabad, Hyderabad 500046, India.
Thaltiri V; Advanced Centre of Research in High Energy Materials, University of Hyderabad, Hyderabad 500046, India.
Balaraju M; Advanced Centre of Research in High Energy Materials, University of Hyderabad, Hyderabad 500046, India.
Sahoo AK; School of Chemistry, University of Hyderabad, Hyderabad 500046, India.; Advanced Centre of Research in High Energy Materials, University of Hyderabad, Hyderabad 500046, India.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 12. Date of Electronic Publication: 2022 May 12.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Pd-Catalyzed Regioselective Intramolecular Allylic C-H Amination of 1,1-Disubstituted Alkenyl Amines.
Autorzy :
Kim YH; Center for New Directions in Organic Synthesis, Department of Chemistry and Research Institute for Natural Sciences, Hanyang University, Seoul 04763, Korea.
Kim DB; Center for New Directions in Organic Synthesis, Department of Chemistry and Research Institute for Natural Sciences, Hanyang University, Seoul 04763, Korea.
Jang SS; Center for New Directions in Organic Synthesis, Department of Chemistry and Research Institute for Natural Sciences, Hanyang University, Seoul 04763, Korea.
Youn SW; Center for New Directions in Organic Synthesis, Department of Chemistry and Research Institute for Natural Sciences, Hanyang University, Seoul 04763, Korea.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 12. Date of Electronic Publication: 2022 May 12.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Multicomponent Synthesis of S -Benzyl Dithiocarbamates from para -Quinone Methides and Their Biological Evaluation for the Treatment of Alzheimer's Disease.
Autorzy :
Venkatesh R; Department of Chemistry, Indian Institute of Technology (BHU), Varanasi, Uttar Pradesh 221005, India.
Shankar G; Department of Pharmaceutical Engineering & Technology, Indian Institute of Technology (Banaras Hindu University), Varanasi 221005, India.
Narayanan AC; Department of Chemistry, Indian Institute of Technology (BHU), Varanasi, Uttar Pradesh 221005, India.
Modi G; Department of Pharmaceutical Engineering & Technology, Indian Institute of Technology (Banaras Hindu University), Varanasi 221005, India.
Sabiah S; Department of Chemistry, Pondicherry University, Pondicherry 605014, India.
Kandasamy J; Department of Chemistry, Indian Institute of Technology (BHU), Varanasi, Uttar Pradesh 221005, India.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 12. Date of Electronic Publication: 2022 May 12.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Difluoromethylarylation of Alkynes from [Bis(difluoroacetoxy)iodo]benzene: Access to CF 2 H-Containing Dibenzazepines.
Autorzy :
Wang L; School of Pharmaceutical and Materials Engineering & Institute for Advanced Studies, Taizhou University, 1139 Shifu Avenue, Taizhou 318000, China.
Zhang Y; School of Pharmaceutical and Materials Engineering & Institute for Advanced Studies, Taizhou University, 1139 Shifu Avenue, Taizhou 318000, China.
Zhu T; School of Pharmaceutical and Materials Engineering & Institute for Advanced Studies, Taizhou University, 1139 Shifu Avenue, Taizhou 318000, China.
Wu J; School of Pharmaceutical and Materials Engineering & Institute for Advanced Studies, Taizhou University, 1139 Shifu Avenue, Taizhou 318000, China.; State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.; School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang 453007, China.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 12. Date of Electronic Publication: 2022 May 12.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Norprzewalsone A, a Rearranged Polycyclic Polyprenylated Acylphloroglucinol with a Spiro[cyclopentane-1,3'-tricyclo[7.4.0.0 ]tridecane] Core from Hypericum przewalskii .
Autorzy :
Duan Y; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Guo Y; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Deng Y; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Bu P; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Shi Z; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Cao Y; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Zhang Y; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Hu H; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Sun W; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Qi C; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Zhang Y; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 12. Date of Electronic Publication: 2022 May 12.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Thionyl Fluoride-Mediated One-Pot Substitutions and Reductions of Carboxylic Acids.
Autorzy :
Bolduc TG; Department of Chemistry, University of British Columbia, Vancouver, British Columbia V6T 1Z1, Canada.
Lee C; Department of Chemistry, University of British Columbia, Vancouver, British Columbia V6T 1Z1, Canada.
Chappell WP; Department of Chemistry, University of British Columbia, Vancouver, British Columbia V6T 1Z1, Canada.
Sammis GM; Department of Chemistry, University of British Columbia, Vancouver, British Columbia V6T 1Z1, Canada.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 12. Date of Electronic Publication: 2022 May 12.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Synthesis of Non-natural Aza-Iridoids via Ynamides and Molecular Networking-Based Tracing of Their In Planta Bioconversion.
Autorzy :
Moegle B; Institut de Chimie, CNRS-UdS, UMR 7177, Equipe Synthèse Organique et Phytochimie, 4 rue Blaise Pascal, CS 90032, 67081 Strasbourg, France.
Hourtoule M; Institut de Chimie, CNRS-UdS, UMR 7177, Equipe Synthèse Organique et Phytochimie, 4 rue Blaise Pascal, CS 90032, 67081 Strasbourg, France.
Gommenginger C; Institut de Chimie, CNRS-UdS, UMR 7177, Equipe Synthèse Organique et Phytochimie, 4 rue Blaise Pascal, CS 90032, 67081 Strasbourg, France.
Belabbes A; Institut de Chimie, CNRS-UdS, UMR 7177, Equipe Synthèse Organique et Phytochimie, 4 rue Blaise Pascal, CS 90032, 67081 Strasbourg, France.
Villette C; Institut de biologie moléculaire des plantes, CNRS, Université de Strasbourg, 12 rue du Général Zimmer, 67084 Strasbourg, France.
Elser D; Institut de biologie moléculaire des plantes, CNRS, Université de Strasbourg, 12 rue du Général Zimmer, 67084 Strasbourg, France.
Gaquerel E; Institut de biologie moléculaire des plantes, CNRS, Université de Strasbourg, 12 rue du Général Zimmer, 67084 Strasbourg, France.
Navrot N; Institut de biologie moléculaire des plantes, CNRS, Université de Strasbourg, 12 rue du Général Zimmer, 67084 Strasbourg, France.
Miesch L; Institut de Chimie, CNRS-UdS, UMR 7177, Equipe Synthèse Organique et Phytochimie, 4 rue Blaise Pascal, CS 90032, 67081 Strasbourg, France.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 12. Date of Electronic Publication: 2022 May 12.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Highly Stereoselective Ugi/Pictet-Spengler Sequence.
Autorzy :
Zhang B; Department of Drug Design, University of Groningen, A. Deusinglaan 1, 9713 AV Groningen, The Netherlands.
Kurpiewska K; Department of Crystal Chemistry and Crystal Physics Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Kraków, Poland.
Dömling A; Department of Drug Design, University of Groningen, A. Deusinglaan 1, 9713 AV Groningen, The Netherlands.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 12. Date of Electronic Publication: 2022 May 12.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Protecting Group-Dependent Synthesis of Densely Substituted Dihydropyrroles v/s Pyrroles via 5 -Exo-trig Cascade Radical Cyclization to Alkynyl Vinylogous Carbamates.
Autorzy :
Gharpure SJ; Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai 400076, India.
Kumari S; Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai 400076, India.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 11. Date of Electronic Publication: 2022 May 11.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Nonenzymatic Asparagine Motif Synthesis by Photoredox-Catalyzed Carbamoylation of Dehydroalanine.
Autorzy :
Guo T; State Key Laboratory of Applied Organic Chemistry, School of Pharmacy, Lanzhou University, Lanzhou 730000, P. R. China.
Wang H; State Key Laboratory of Applied Organic Chemistry, School of Pharmacy, Lanzhou University, Lanzhou 730000, P. R. China.
Wang C; School of Environmental and Chemical Engineering, Lanzhou Resources & Environment Voc-Tech College, Lanzhou 730021, P. R. China.
Tang S; State Key Laboratory of Applied Organic Chemistry, School of Pharmacy, Lanzhou University, Lanzhou 730000, P. R. China.
Liu J; State Key Laboratory of Applied Organic Chemistry, School of Pharmacy, Lanzhou University, Lanzhou 730000, P. R. China.
Wang X; State Key Laboratory of Applied Organic Chemistry, School of Pharmacy, Lanzhou University, Lanzhou 730000, P. R. China.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 10. Date of Electronic Publication: 2022 May 10.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Synthesis of Benzothiophene-3-carboxylic Esters by Palladium Iodide-Catalyzed Oxidative Cyclization-Deprotection-Alkoxycarbonylation Sequence under Aerobic Conditions.
Autorzy :
Mancuso R; Laboratory of Industrial and Synthetic Organic Chemistry (LISOC), Department of Chemistry and Chemical Technologies, University of Calabria, Via Pietro Bucci 12/C, 87036 Arcavacata di Rende (CS), Italy.
Cuglietta S; Laboratory of Industrial and Synthetic Organic Chemistry (LISOC), Department of Chemistry and Chemical Technologies, University of Calabria, Via Pietro Bucci 12/C, 87036 Arcavacata di Rende (CS), Italy.
Strangis R; Laboratory of Industrial and Synthetic Organic Chemistry (LISOC), Department of Chemistry and Chemical Technologies, University of Calabria, Via Pietro Bucci 12/C, 87036 Arcavacata di Rende (CS), Italy.
Gabriele B; Laboratory of Industrial and Synthetic Organic Chemistry (LISOC), Department of Chemistry and Chemical Technologies, University of Calabria, Via Pietro Bucci 12/C, 87036 Arcavacata di Rende (CS), Italy.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 10. Date of Electronic Publication: 2022 May 10.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Stereoselective Synthesis of β-d-Manno-heptopyranoside via Cs 2 CO 3 -Mediated Anomeric O -Alkylation: Synthesis of a Tetrasaccharide Repeat Unit of Bacillus thermoaerophilus Surface-Layer Glycoprotein.
Autorzy :
Meng S; Department of Chemistry and Biochemistry and School of Green Chemistry and Engineering, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio 43606, United States.
Hettiarachchi IL; Department of Chemistry and Biochemistry and School of Green Chemistry and Engineering, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio 43606, United States.
Bhetuwal BR; Department of Chemistry and Biochemistry and School of Green Chemistry and Engineering, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio 43606, United States.
Thapa P; Department of Chemistry and Biochemistry and School of Green Chemistry and Engineering, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio 43606, United States.
Zhu J; Department of Chemistry and Biochemistry and School of Green Chemistry and Engineering, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio 43606, United States.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 May 10. Date of Electronic Publication: 2022 May 10.
Typ publikacji :
Journal Article
Czasopismo naukowe

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