ECSOC-25Pub Date : 2021-11-14DOI: 10.3390/ecsoc-25-11700
Vanina A. Guntero, C. Ferretti
{"title":"Valorization of Orange Peels as a Source of Pectins","authors":"Vanina A. Guntero, C. Ferretti","doi":"10.3390/ecsoc-25-11700","DOIUrl":"https://doi.org/10.3390/ecsoc-25-11700","url":null,"abstract":"","PeriodicalId":11441,"journal":{"name":"ECSOC-25","volume":"104 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76222139","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
ECSOC-25Pub Date : 2021-11-14DOI: 10.3390/ecsoc-25-11706
N. Medjahed, Z. Kibou, A. Berrichi, R. Bachir, N. Choukchou-Braham
{"title":"Synthesis of Bis-Hydrazine Using Heterogeneous Catalysis","authors":"N. Medjahed, Z. Kibou, A. Berrichi, R. Bachir, N. Choukchou-Braham","doi":"10.3390/ecsoc-25-11706","DOIUrl":"https://doi.org/10.3390/ecsoc-25-11706","url":null,"abstract":": Hydrazine derivatives are known as a group of organic compounds containing C=N-N=C functional groups. This π -conjugated system enables electronic excitation in the visible and near-ultraviolet regions. This is of particular interest for many applications, such as corrosion inhibition dye-sensitized solar cells (DSSC), organogels, and fluorescent probes for analytical testing. In addition, many hydrazine derivatives show notable biological and therapeutic activities such as the treatment of tuberculosis, Parkinson’s disease, and hypertension. Schiff bases form a remarkable class of ligands because of their unique properties, such as stability under different conditions, diversity of donor sites, the flexibility of synthesis, and formation of ranges in various coordination geometries in a wide range of complexes. Their complexes have received widespread attention due to their wide range of applications, such as catalysis, electrochemistry, biological sciences, optics, guest chemistry, and molecular recognition. Therefore, from theoretical and practical points of view, the synthesis of hydrazine derivatives is an important issue. In the present study, we describe a new, efficient, and environmentally benign synthetic method for the formation of hydrazine derivatives with heterogeneous catalysis starting from ketones.","PeriodicalId":11441,"journal":{"name":"ECSOC-25","volume":"174 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75711596","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
ECSOC-25Pub Date : 2021-11-14DOI: 10.3390/ecsoc-25-11764
S. Patil, P. Bhatt, H. Suryawanshi, J. Patil, Rajesh Chaudhari
{"title":"Synthesis and Biological Evaluation of Some Substituted Benzimidazole Derivatives","authors":"S. Patil, P. Bhatt, H. Suryawanshi, J. Patil, Rajesh Chaudhari","doi":"10.3390/ecsoc-25-11764","DOIUrl":"https://doi.org/10.3390/ecsoc-25-11764","url":null,"abstract":"","PeriodicalId":11441,"journal":{"name":"ECSOC-25","volume":"30 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84368566","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
ECSOC-25Pub Date : 2021-11-14DOI: 10.3390/ecsoc-25-11701
César Ray, Carolina Díaz-Norambuena, C. Schad, Florencio Moreno, A. R. Agarrabeitia, M. Ortiz, T. Arbeloa, J. Bañuelos, B. L. Maroto, S. D. L. Moya
{"title":"Influence of At-Bridge Nitro Groups on the Photophysics and Chiroptics of helicoBODIPYs: A Step Forward towards the Development of New Chiroptical Sensors","authors":"César Ray, Carolina Díaz-Norambuena, C. Schad, Florencio Moreno, A. R. Agarrabeitia, M. Ortiz, T. Arbeloa, J. Bañuelos, B. L. Maroto, S. D. L. Moya","doi":"10.3390/ecsoc-25-11701","DOIUrl":"https://doi.org/10.3390/ecsoc-25-11701","url":null,"abstract":": A new helicoBODIPY (bisBODIPY with helical chirality) with nitro groups at the chiral bridge has been synthesized as a model to study the influence of the at-bridge substitution on the photophysics and chiroptics of the helicoBODIPY. This preliminary study reveals that at-bridge substitution can be a strategy for the development of chiroptical sensors based on helicoBODIPYs.","PeriodicalId":11441,"journal":{"name":"ECSOC-25","volume":"69 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85628804","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
ECSOC-25Pub Date : 2021-11-14DOI: 10.3390/ecsoc-25-11776
P. Kovyazin, P. Ivchenko, I. Nifant’ev, L. Parfenova
{"title":"Synthesis of Dibenzylbutane and 9,8′-Neo-Lignans via Cyclometalation of Allylbenzene by EtAlCl2 and Mg in the Presence of Zr ansa-Complexes","authors":"P. Kovyazin, P. Ivchenko, I. Nifant’ev, L. Parfenova","doi":"10.3390/ecsoc-25-11776","DOIUrl":"https://doi.org/10.3390/ecsoc-25-11776","url":null,"abstract":"","PeriodicalId":11441,"journal":{"name":"ECSOC-25","volume":"18 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76103743","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
ECSOC-25Pub Date : 2021-11-14DOI: 10.3390/ecsoc-25-11703
Assia Chebieb, C. Ziani-Chérif, Khadidja Bellifa
{"title":"In-Silico Studies toward the Improvement of the Antibacterial Activity of Pristinamycin IIB","authors":"Assia Chebieb, C. Ziani-Chérif, Khadidja Bellifa","doi":"10.3390/ecsoc-25-11703","DOIUrl":"https://doi.org/10.3390/ecsoc-25-11703","url":null,"abstract":": Pristinamycin IIB (PIIB) is a potent antibiotic with limited use, due to some structural problems and also due to the bacterial resistance exhibited toward the antibiotic. A thorough study led to the design of novel analogues of PIIB, based on the introduction of a difluorostatone moiety. Herein, we describe the initial in silico studies toward these novel analogues using ADMET modeling of predictive models in order to compute the physicochemistry and estimate the pharmacokinetics, drug-likeness and medicinal chemistry friendliness of these newly designed analogues.","PeriodicalId":11441,"journal":{"name":"ECSOC-25","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89745922","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
ECSOC-25Pub Date : 2021-11-14DOI: 10.3390/ecsoc-25-11689
C. Teixeira, Nuno F S Pinto, David M. Pereira, R. Pereira, M. J. Fernandes, E. M. Castanheira, A. Fortes, M. S. Gonçalves
{"title":"Cytotoxicity Studies of Eugenol Amino Alcohols Derivatives","authors":"C. Teixeira, Nuno F S Pinto, David M. Pereira, R. Pereira, M. J. Fernandes, E. M. Castanheira, A. Fortes, M. S. Gonçalves","doi":"10.3390/ecsoc-25-11689","DOIUrl":"https://doi.org/10.3390/ecsoc-25-11689","url":null,"abstract":": Eugenol is a phenylpropanoid displaying a wide range of biological activities. In this study, the cytotoxic activity of various β -amino alcohols derivatives from eugenol was evaluated in AGS (gastric cancer) and A549 (lung cancer) cell lines. The results show that some structural modi-fications resulted in enhanced cytotoxic activity towards cancer cells. In addition, the activation of caspase-3 and hence apoptosis induced by these molecules, was also explored. Considering the ob-tained results, some structure/activity relationships can be drawn, which may guide future structural improvements for anticancer agents.","PeriodicalId":11441,"journal":{"name":"ECSOC-25","volume":"14 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89738434","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
ECSOC-25Pub Date : 2021-11-14DOI: 10.3390/ecsoc-25-11774
Yemin Zheng, Jaime A. Martinez‐Acosta, Mohammed Khimji, L. Barbosa, G. Clarkson, M. Wills
{"title":"Asymmetric Transfer Hydrogenation of Aryl Heteroaryl Ketones and o-Hydroxyphenyl Ketones Using Noyori-Ikariya Catalysts","authors":"Yemin Zheng, Jaime A. Martinez‐Acosta, Mohammed Khimji, L. Barbosa, G. Clarkson, M. Wills","doi":"10.3390/ecsoc-25-11774","DOIUrl":"https://doi.org/10.3390/ecsoc-25-11774","url":null,"abstract":"","PeriodicalId":11441,"journal":{"name":"ECSOC-25","volume":"101 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73535624","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
ECSOC-25Pub Date : 2021-11-14DOI: 10.3390/ecsoc-25-11704
I. Islamov, A. Yusupova, L. Dzhemileva, U. Dzhemilev
{"title":"Targeted Synthesis and Antitumor Activity In Vitro Macrodiolides Containing 1Z,5Z-Diene and 1,3-Diyne Moieties","authors":"I. Islamov, A. Yusupova, L. Dzhemileva, U. Dzhemilev","doi":"10.3390/ecsoc-25-11704","DOIUrl":"https://doi.org/10.3390/ecsoc-25-11704","url":null,"abstract":"","PeriodicalId":11441,"journal":{"name":"ECSOC-25","volume":"6 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90967293","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
ECSOC-25Pub Date : 2021-11-14DOI: 10.3390/ecsoc-25-11715
Mariana Celman, Leandro G. Gutierrez, Carla M. Ormachea, C. Ferretti
{"title":"Evaluation of the Recovery of Furfural from Wood Scraps","authors":"Mariana Celman, Leandro G. Gutierrez, Carla M. Ormachea, C. Ferretti","doi":"10.3390/ecsoc-25-11715","DOIUrl":"https://doi.org/10.3390/ecsoc-25-11715","url":null,"abstract":": 2-furfuraldehyde, commonly known as furfural, is a product of the hydrolysis and dehydration of pentose carbohydrates contained in lignocellulosic. Furfural is currently a commodity chemical, identified as one of the most promising chemical platforms directly derived from biomass, to produce chemicals, biofuels, and additives. Wood scraps are a good source of natural pentoses that contains up to 25%. Taking this into account, the goal of the research was to evaluate the recovery of furfural from wood scraps. The process of recovery of furfural was carried out by acid-catalyzed pentoses dehydration, associated with a hydrodistillation. As a catalyst, we used a solution of hydrochloric acid of 10% wt. The physicochemical analysis of the samples obtained allowed us to characterize and evaluate the recovery process. The results showed that under the experimental conditions evaluated, the degree of recovery of furfural was about 5%.","PeriodicalId":11441,"journal":{"name":"ECSOC-25","volume":"27 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80219257","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}