Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Cagatay Dengiz"'
Autor:
Cagatay Dengiz
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 19, Iss 1, Pp 1895-1911 (2023)
There has been a growing emphasis on the synthesis of polycyclic conjugated compounds, driven by their distinct structural characteristics that make them valuable candidates for use in cutting-edge technologies. In particular, acenes, a subgroup of p
Externí odkaz:
https://doaj.org/article/aec70c62e4e24a508de7acc7df6ed594
Publikováno v:
SynOpen, Vol 07, Iss 01, Pp 1-7 (2023)
Homoconjugated push–pull chromophores were obtained by an efficient, click-type formal [2+2] cycloaddition. With these short synthetic transformations, complex chromophore structures were achieved in a single step without any by-product formation.
Externí odkaz:
https://doaj.org/article/625cdd39ad334b4ca1e91ebc17fbd562
Autor:
Ebru Koçak Aslan, Muhammed İhsan Han, Vagolu Siva Krishna, Rasoul Tamhaev, Cagatay Dengiz, Şengül Dilem Doğan, Christian Lherbet, Lionel Mourey, Tone Tønjum, Miyase Gözde Gündüz
Publikováno v:
Pharmaceuticals, Vol 15, Iss 10, p 1301 (2022)
Isoniazid (INH) is one of the key molecules employed in the treatment of tuberculosis (TB), the most deadly infectious disease worldwide. However, the efficacy of this cornerstone drug has seriously decreased due to emerging INH-resistant strains of
Externí odkaz:
https://doaj.org/article/a33981310c2b4397b04312c17265e4aa
Publikováno v:
SynOpen. :1-7
Homoconjugated push–pull chromophores were obtained by an efficient, click-type formal [2+2] cycloaddition. With these short synthetic transformations, complex chromophore structures were achieved in a single step without any by-product formation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3d56293a263c58d868acccd91ab2621
https://doi.org/10.1055/a-2004-6344
https://doi.org/10.1055/a-2004-6344
Publikováno v:
The Journal of Organic Chemistry. 86:2489-2498
This manuscript details the development of a general and mild protocol for the α-C-H cyanation of tertiary amines and its application in late-stage functionalization. Suitable substrates include tertiary aliphatic, benzylic, and aniline-type substra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd366d0b3763a8499a649c63aca2507f
https://doi.org/10.1021/acs.joc.0c02642
https://doi.org/10.1021/acs.joc.0c02642
Autor:
Cagatay Dengiz, KÜBRA ERDEN
Publikováno v:
The Journal of organic chemistry. 87(6)
In this study, two different classes of push-pull chromophores were synthesized in modest to excellent yields by formal [2+2] cycloaddition-retroelectrocyclization (CA-RE) reactions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fe2f4cc531c42de96e75f1f820698b2
https://pubmed.ncbi.nlm.nih.gov/35230842
https://pubmed.ncbi.nlm.nih.gov/35230842
Publikováno v:
Archives of Microbiology. 202:2401-2409
In this study, the structure of the purified extracellular eumelanin pigment isolated from Streptomyces spp. was elucidated by detailed analysis via two different spectroscopic techniques (FT-IR and NMR). In vitro antiproliferative effects of eumelan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a51fdb17c31df0edfa3e0a006236e2d0
https://doi.org/10.1007/s00203-020-01956-2
https://doi.org/10.1007/s00203-020-01956-2
Publikováno v:
Dyes and Pigments. 209:110894
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::057f4da9a37b316a4b46bf350353cd50
https://doi.org/10.1016/j.dyepig.2022.110894
https://doi.org/10.1016/j.dyepig.2022.110894
Publikováno v:
Tetrahedron Letters. 60:1982-1985
1-(4-Ethynylphenyl)-3,3-dialkyltriaz-1-enes, well-known building blocks for branched dendrimer syntheses, were utilized as a new type of electron-donor component in formal [2 + 2] cycloadditions. The click-type, atom-economic reactions proceed effici
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43156feff40697e6e1dce98501292edd
https://doi.org/10.1016/j.tetlet.2019.06.046
https://doi.org/10.1016/j.tetlet.2019.06.046
Publikováno v:
Synlett. 30:54-58
We report the synthesis and characterization of iptycene–naphthazarin dyes by using a sequential Diels–Alder approach. The tautomerization of naphthazarin was used as the key step in the synthesis, with structures confirmed by single-crystal X-ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9dbd14d0d5d218120791b5ab7797e8d1
https://doi.org/10.1055/s-0037-1611169
https://doi.org/10.1055/s-0037-1611169