Zobrazeno 1 - 10
of 21
pro vyhledávání: '"A. A. Arbale"'
Autor:
Karakus, Gozde Sir, Tastan, Cihan, Kancagi, Derya Dilek, Yurtsever, Bulut, Tumentemur, Gamze, Demir, Sevda, Turan, Raife Dilek, Abanuz, Selen, Cakirsoy, Didem, Seyis, Utku, Ozer, Samed, Elibol, Omer, Elek, Muhammer, Ertop, Gurcan, Arbale, Serap, Elmas, Merve Acikel, Hermsinlioglu, Canso, Kocagoz, Ayse Sesin, Ng, Ozden Hatirnaz, Akyoney, Sezer
COVID-19 outbreak caused by SARS-CoV-2 created an unprecedented health crisis since there is no vaccine for this novel virus. Therefore, SARS-CoV-2 vaccines have become crucial for reducing morbidity and mortality. In this study, in vitro and in vivo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=r39c86a4b39b::b6f91289d9c606314fb993b00a97607c
https://aperta.ulakbim.gov.tr/record/231896
https://aperta.ulakbim.gov.tr/record/231896
Publikováno v:
ChemInform. 22
Publikováno v:
Synthetic Communications. 20:2217-2223
A simple facile synthesis of 2,2-dichloro-spiro (2,5)-octane-1-carboxylic acid has been described which was converted into the corresponding α (RS) cyano 3-phenoxybenzyl ester, exhibiting high insecticidal activity against Musca domestica and Aedes
Publikováno v:
Synthetic Communications. 20:839-847
A simple route is described for the synthesis of 1,2 Seco-chrysanthemic acid and their structural analogues, employing Claisen orthoester rearrangement reaction in the key-step of synthesis. These acids have been prepared with a view to evaluating so
Publikováno v:
ChemInform. 21
A simple route is described for the synthesis of 1,2 Seco-chrysanthemic acid and their structural analogues, employing Claisen orthoester rearrangement reaction in the key-step of synthesis. These acids have been prepared with a view to evaluating so
Publikováno v:
ChemInform. 21
Akademický článek
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Publikováno v:
Synthetic Communications; Jul1990, Vol. 20 Issue 14, p2217-2223, 7p
Publikováno v:
Synthetic Communications; Mar1990, Vol. 20 Issue 6, p839-847, 9p
Autor:
Kulkarni, G. H., Arbale, A. A.
Publikováno v:
Synthetic Communications; Nov1988, Vol. 18 Issue 16/17, p2147-2159, 13p