Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Martin Bělohradský"'
Autor:
Sónia Pérez-Rentero, Alvaro Somoza, Santiago Grijalvo, Jiří Janoušek, Martin Bělohradský, Irena G. Stará, Ivo Starý, Ramon Eritja
Publikováno v:
Journal of Chemistry, Vol 2013 (2013)
Oligonucleotide conjugates carrying a single functionalized tetrathiafulvalene (TTF) unit linked through a threoninol molecule to the 3′ or 5′ ends were synthesized together with their complementary oligonucleotides carrying a TTF, pyrene, or pen
Externí odkaz:
https://doaj.org/article/72326e6451cb4deda29b99480eddde93
Autor:
Lubomír Pospíšil, Irena G. Stará, Jaroslav Vacek, Martin Bělohradský, Jana Vacek Chocholoušová, Magdaléna Hromadová, Jan Fiedler, Radek Pohl, Šárka Lipnická, Ivo Starý, Viliam Kolivoška
Publikováno v:
Chemistry - A European Journal. 19:6108-6121
Short monodisperse oligo- (para-phenyleneethynylene) (pOPE) units bearing laterally attached tetrathio-substituted tetrathiofulvalene (TTF) units have been synthesised from functionalised aromatic building blocks by using the Sonogashira cross-coupli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d3edc939b44144e06b1e77fec4fc36c
https://doi.org/10.1002/chem.201102868
https://doi.org/10.1002/chem.201102868
Autor:
Jiří Janoušek, Ivo Starý, Álvaro Somoza, Ramon Eritja, Irena G. Stará, Martin Bělohradský, Sónia Pérez-Rentero, Santiago Grijalvo
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Journal of Chemistry, Vol 2013 (2013)
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
instname
Journal of Chemistry, Vol 2013 (2013)
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
Oligonucleotide conjugates carrying a single functionalized tetrathiafulvalene (TTF) unit linked through a threoninol molecule to the 3′ or 5′ ends were synthesized together with their complementary oligonucleotides carrying a TTF, pyrene, or pen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e9053fec5d4b3d7c8926f98b98bb18d
https://doi.org/10.1155/2013/650610
https://doi.org/10.1155/2013/650610
Publikováno v:
Separation Science and Technology. 46:2174-2182
New methods of extraction of 137Cs and 85Sr into solvent mixture of dodecanenitrile with n-dodecane in the presence of various crown ethers and chlorinated dicarbollide are described. This is the first time when extraction with chlorinated dicarbolli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::390619df2c9e68c5b779fe326e84cfcd
https://doi.org/10.1080/01496395.2011.594849
https://doi.org/10.1080/01496395.2011.594849
Autor:
Martin Bělohradský, Petr Holý, Martin Høj, Jiří Rybáček, Kristine Kilså, Markéta Rybáčková, Mogens Brøndsted Nielsen
Publikováno v:
Tetrahedron. 63:8840-8854
A large selection of triptycenes functionalized with tetrathiafulvalene (TTF) units as well as triptycenes containing extended TTFs as a part of the triptycene core have been synthesized utilizing new triptycene di- and tetraaldehydes as well as bis-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e2e45f131b18b19228797f83e45c6b2
https://doi.org/10.1016/j.tet.2007.06.020
https://doi.org/10.1016/j.tet.2007.06.020
Publikováno v:
Synthesis. 2007:1554-1558
Two alternative procedures, both starting from easily accessible- tetramethylanthracenes and employing the Diels-Alder addition as the key reaction step(s), have been examined in the synthesis of the title compounds.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df43a30fab7b8d0663ff1cb68e7f42ca
https://doi.org/10.1055/s-2007-966042
https://doi.org/10.1055/s-2007-966042
Publikováno v:
Synthesis. 2006:2039-2042
A simple two-step synthesis of triptycene di- and tetracarboxylic acids is reported. Diels-Alder reaction between dimethylanthracenes and appropriate arynes, generated in situ from anthranilic or dimethylanthranilic acid, afforded di- or tetramethyl-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0127c2e2087dcc70402921dde6b4a8a7
https://doi.org/10.1055/s-2006-942385
https://doi.org/10.1055/s-2006-942385
Autor:
Jiří Báča, Jaromír Plešek, Véronique Lamare, Jean Francois Dozol, Martin Bělohradský, Bohumír Grüner, Josef Čáslavský, Ivana Císařová
Publikováno v:
New Journal of Chemistry. 26:867-875
A series of crown ether derivatives of the cobalta bis(dicarbollide) closo-[(1,2-C2B9H11)2-3,3′-Co]− (1) anion was prepared using two synthetic strategies. The first method employs dioxane ring cleavage of the closo-[{8-(C4H8O2)-1,2-C2B9H10}-3,3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc6e6972e9c67c7c76aad5c90fc7e36a
https://doi.org/10.1039/b109956f
https://doi.org/10.1039/b109956f
Publikováno v:
Collection of Czechoslovak Chemical Communications. 67:1719-1728
Five potential molecular shuttles based on degenerate [2]rotaxanes - wherein the ring component is a bis-1,4-phenylene[34]crown-10 and the dumbbell components are terminated by tetraarylmethane (slippage) stoppers and contain two identical bipyridini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8df17400e1460aae04327a0b46860387
https://doi.org/10.1135/cccc20021719
https://doi.org/10.1135/cccc20021719
Autor:
Stephan Menzer, J. Fraser Stoddart, and Andrew N. Shipway, Martin Bělohradský, David J. Williams, Christoph Hamers, and Andrew J. P. White, Françisco M. Raymo
Publikováno v:
Macromolecules. 31:295-307
A series of mono- and difunctionalized [2]catenanes, incorporating a bipyridinium-based cyclophane component interlocked with a dioxyarene-based macrocyclic polyether, have been self-assembled. The methodology relies upon the complementarity between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35d3273783af6d736683c53e887767b0
https://doi.org/10.1021/ma970685w
https://doi.org/10.1021/ma970685w