Zobrazeno 1 - 10
of 152
pro vyhledávání: '"Carbon Nuclear Magnetic Resonance"'
Autor:
Drewes, Jörg E., Fox, Peter
Publikováno v:
Water Environment Research, 2000 May 01. 72(3), 353-362.
Externí odkaz:
https://www.jstor.org/stable/25045386
Autor:
G. Suresh, Wudayagiri Rajendra, Chintha Venkataramaiah, N. Bakthavatchala Reddy, Grigory V. Zyryanov, C. Suresh Reddy, Avula Balakrishna, G. Sravya, K. Madhu Kumar Reddy
Publikováno v:
Journal of Heterocyclic Chemistry
A simple method was employed for the synthesis of dihydropyrano[3, 2-b]chromenedione derivatives (4a-o) in high yields by condensation of 5, 5-dimethylcyclohexane-1, 3-dione(1), different aromatic aldehydes (2a-o), and 5-hydroxy-2-(hydroxymethyl)-4H-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1601b55f3b3dda872e0c9bdf3ca67d35
https://doi.org/10.1002/jhet.3786
https://doi.org/10.1002/jhet.3786
Akademický článek
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Autor:
Alexander Spasov, Vadim Kosolapov, Denis Babkov, Vladlen Klochkov, Elena Sokolova, Mikhail Miroshnikov, Alexander Borisov, Yulia Velikorodnaya, Alexey Smirnov, Konstantin Savateev, Victor Fedotov, Svetlana Kotovskaya, Vladimir Rusinov
Publikováno v:
Pharmaceuticals; Volume 15; Issue 5; Pages: 537
Pharmaceuticals
Pharmaceuticals
Acute lung injury remains a challenging clinical condition, necessitating the development of novel, safe and efficient treatments. The prevention of macrophage M1-polarization is a viable venue to tackle excessive inflammation. We performed a phenoty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9044e985f053840f3b814bc392bc5c7
https://doi.org/10.3390/ph15050537
https://doi.org/10.3390/ph15050537
Autor:
Marco Consumi, Claudio Rossi, Agnese Magnani, Alessandro Donati, Gabriella Tamasi, Alessio Pardini, Claudia Bonechi, Gemma Leone
Nuclear magnetic resonance spectroscopy is a straightforward technique for studying molecular dynamics that range in timescale from picosecond (motions faster than molecular reorientation) to those that occur in real-time. This approach is important
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e64f55497e5a4ab87720fd3fc194a5f
http://hdl.handle.net/11365/1072187
http://hdl.handle.net/11365/1072187
Publikováno v:
Medicinal Chemistry Research. 27:634-641
WOS: 000424646600026
In this study we report that amino acridine intermediates 7 and 8 were obtained from the reduction of nitro acridine derivatives 5 and 6 that were synthesized via the condensation of dimedone, p-nitrobenzaldehyde with variou
In this study we report that amino acridine intermediates 7 and 8 were obtained from the reduction of nitro acridine derivatives 5 and 6 that were synthesized via the condensation of dimedone, p-nitrobenzaldehyde with variou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1db601d11c96e57aa2bde16aa7f43064
https://doi.org/10.1007/s00044-017-2088-2
https://doi.org/10.1007/s00044-017-2088-2
Publikováno v:
Drug Testing and Analysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0056627257cd8e02ca40ab7f8f0c9260
https://elar.urfu.ru/handle/10995/90257
https://elar.urfu.ru/handle/10995/90257
Autor:
Swetha Vallela, Visweswara Rao Pasupuleti, Grigoriy V. Zyryanov, Venkataramana Lachhi Reddy, Naga Raju Chamarthi, Jaya Shree Anireddy, Vijay Kumar Reddy Avula
Publikováno v:
Bioorg. Chem.
Bioorganic Chemistry
Bioorganic Chemistry
A series of 1-(2,3-dihydro-1H-indan-1-yl)-3-aryl urea/thiourea derivatives (4a-j) have been synthesized from the reaction of 2,3-dihydro-1H-inden-1-amine (2) with various aryl isocyanates/isothiocyanates (3a-j) by using N,N-DIPEA base (Hunig's base)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fc0762df3d5d57522edfdd207388aa1
https://pubmed.ncbi.nlm.nih.gov/31911311
https://pubmed.ncbi.nlm.nih.gov/31911311
In this study, seven new 3(2H)-pyridazinone derivatives expected to show cytotoxic activity in liver and colon cancer cell lines were synthesized. Their structures were confirmed by the IR, 1 H-NMR, 13 C-NMR spectra and elementary analyses. Compunds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::433a8c4dcdaf40134925ded05db827ad
https://avesis.gazi.edu.tr/publication/details/2f74ddc1-b116-42a9-bbdd-db5d4505edf2/oai
https://avesis.gazi.edu.tr/publication/details/2f74ddc1-b116-42a9-bbdd-db5d4505edf2/oai
Publikováno v:
Synthesis, 48(8), 1122-1130. GEORG THIEME VERLAG KG
We describe the hitherto unknown use of N-Boc-protected hydrazine in the Ugi tetrazole reaction to access a library of highly substituted 5-(hydrazinomethyl)-1-methyl-1H-tetrazoles. The reaction is very versatile and good to high yielding. A one-pot,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0cdd67e04d29021cee37957a4d07333
https://research.rug.nl/en/publications/539d7505-f8f8-4c3c-a96d-9570d4589751
https://research.rug.nl/en/publications/539d7505-f8f8-4c3c-a96d-9570d4589751