Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Mladen Vinković"'
Publikováno v:
Acta Crystallographica Section E, Vol 66, Iss 5, Pp o1098-o1099 (2010)
There are two independent molecules per asymmetric unit of the title compound, C26H23N2O3PS. Their superposition shows that they differ in the conformation of the CH3CO– group and the benzene rings from the triphenylphosphorane group. In the crysta
Externí odkaz:
https://doaj.org/article/6a875e104dd54ceea112a552aefefbf1
Autor:
Kai Wu, Tanya K. Ronson, Leonard Goh, Weichao Xue, Andrew W. Heard, Pingru Su, Xiaopeng Li, Mladen Vinković, Jonathan R. Nitschke
Publikováno v:
Journal of the American Chemical Society. 145:11356-11363
The allosteric regulation of biomolecules, such as enzymes, enables them to adapt and alter their conformation to fit specific substrates, expressing different functionalities in response to stimuli. Different stimuli can also trigger synthetic coord
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa111795c140a474eb85bdb3752ff7e6
https://doi.org/10.1021/jacs.3c02491
https://doi.org/10.1021/jacs.3c02491
Autor:
Kai Wu, Tanya K. Ronson, Pingru Su, Zhi Chen, Leonard Goh, Andrew W. Heard, Xiaopeng Li, Fabian Klautzsch, Christoph A. Schalley, Mladen Vinković, Jonathan R. Nitschke
Biological encapsulants, such as viral capsids and ferritin protein cages, use many identical subunits to tile the surface of a polyhedron. Inspired by these natural systems, synthetic chemists have prepared an extensive series of artificial nanocage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2374e803072bb3f55db50abde44abc5
https://doi.org/10.26434/chemrxiv-2022-p836x
https://doi.org/10.26434/chemrxiv-2022-p836x
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :1944-1950
A combined use of NMR spectroscopy and molecular modelling has enabled insight into conformational features of the novel sugar–peptide adducts 1–3. Cyclic neoglycopeptide 1, having the β-D-glucopyranose moiety which connects terminal parts of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52ab0606e553695aa2f0db6ed2b1b686
https://doi.org/10.1039/b104239b
https://doi.org/10.1039/b104239b
Publikováno v:
Tetrahedron. 51:5083-5092
The enantiomerically pure 2-azacepham sulfoxide 2a was synthesized by stereocontrolled intramolecular cyclization of sulfinates 3 or sulfinamides 8 in the presence of dry hydrogen chloride followed by triethylamine. The cyclization accrued via equili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0629389b49c7c0f5b8fd1ab37b1b4da0
https://doi.org/10.1016/0040-4020(95)98705-m
https://doi.org/10.1016/0040-4020(95)98705-m
Publikováno v:
Tetrahedron: Asymmetry. 5:1605-1612
The enantiomerically pure substituted 2-azacephams 5 were synthesized by intramolecular cyclization of sulfinamides 4. Their absolute configurations were confirmed by X-ray crystal structure determination of (5R,6R)-4-benzyl-2-isopropylidene-5-oxo-5-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5da69b4d1e4d2a739d30a9d0c4aee10f
https://doi.org/10.1016/0957-4166(94)80131-2
https://doi.org/10.1016/0957-4166(94)80131-2
Publikováno v:
Tetrahedron. 50:12201-12210
The conformation of 9a- 4 and 8a- 5 bicyclic iminoethers, the key synthetic intermediates of 15-membered AZALIDES was determined. The 2D NMR data and molecular modeling techniques were used to establish the predominant solution-state conformation. Co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba7770be62cd7f13c3bec10781984c72
https://doi.org/10.1016/s0040-4020(01)89570-3
https://doi.org/10.1016/s0040-4020(01)89570-3
Autor:
Dražen Vikić-Topić, Gabrijela Kobrehel, Biserka Metelko, Mladen Vinković, Gorjana Lazarevski, Slobodan Đokić
Publikováno v:
Tetrahedron. 49:721-730
The conformation of azithromycin 1 in the solution was determined by NMR spectroscopy and molecular mechanics calculations and compared with its crystal structure and with some erythromycin derivatives. In solution 1 exists predominantly in a “fold
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e69c831aacc6d05f54d529d7b795fb5a
https://doi.org/10.1016/s0040-4020(01)86274-8
https://doi.org/10.1016/s0040-4020(01)86274-8
Publikováno v:
ChemInform. 26
The enantiomerically pure substituted 2-azacephams 5 were synthesized by intramolecular cyclization of sulfinamides 4. Their absolute configurations were confirmed by X-ray crystal structure determination of (5R,6R)-4-benzyl-2-isopropylidene-5-oxo-5-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5be40c34b171fb944c0f940a9d82cb1
https://doi.org/10.1002/chin.199503255
https://doi.org/10.1002/chin.199503255
Publikováno v:
Croatica Chemica Acta
Volume 79
Issue 2
Volume 79
Issue 2
Chemo-selective synthesis and characterization of N-[(4-nitrophenyl)sulphanyl]- 2 and N-[(4- nitrophenyl)sulphinyl]- 3 N-[(4-aminophenyl)sulphonyl]- 5 and N-(4-aminobenzoyl)- 7 derivatives of 1a,2,6,6a-tetrahydro-1H,4H-[1,3]dioxepino[5,6-b]azirines,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______951::12bd5619ddc9e1d919fa5742f93125ee
https://hrcak.srce.hr/file/6797
https://hrcak.srce.hr/file/6797