Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Gabriella Mezey-Vándor"'
Autor:
Jerald S. Bradshaw, Péter Huszthy, Gabriella Mezey-Vándor, Reed M. Izatt, Erika Samu, Mihály Nógrádi, Borbála Vermes
Publikováno v:
Tetrahedron. 55:1491-1504
Novel acridino- and phenazino-18-crown-6 ligands 5 and 6 were prepared from acridine-4,5-diol (9) and phenazine-1,9-diol (10) with tetraethylene glycol di-p-tosylate (11) using potassium teri-butoxide as a base in THF. New optically pure dimethyl-sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::656255e04789ee351c4e42fc03c27f22
https://doi.org/10.1016/s0040-4020(98)01128-4
https://doi.org/10.1016/s0040-4020(98)01128-4
Publikováno v:
Monatshefte f�r Chemie Chemical Monthly. 125:425-432
During ketalization with ethyleneglycol an arylideneacetone1 dimerized via its ketal2 to give a 4-acetyl-3,5-diarylcyclohexanone ketal5.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63ee872f6abd83dd8149e245c5fe292b
https://doi.org/10.1007/bf00811860
https://doi.org/10.1007/bf00811860
Publikováno v:
Tetrahedron. 49:4893-4900
The Z isomer of the title compound (21) and its regioisomer (22) were synthesized using an isoxazole synthon (17) for the elaboration of the β-methoxy-enone function. 21 and 20 spontaneously isomerized to the E isomers i.e. to garugamblin-1 (1) and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08bdfdd2a77789309e7c03ac8fa42433
https://doi.org/10.1016/s0040-4020(01)80406-3
https://doi.org/10.1016/s0040-4020(01)80406-3
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c336ed078b6b5f0e751388fe1343cdfd
https://doi.org/10.1002/chin.199221296
https://doi.org/10.1002/chin.199221296
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a6de716891a706a252c9e88eed06f25
https://doi.org/10.1002/chin.199339294
https://doi.org/10.1002/chin.199339294
Autor:
B. Vermes, Gabriella Mezey-Vándor, L. Kametler, György M. Keserü, Mihály Nógrádi, Mária Kajtár-Peredy
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39ac3d35ca0f3861df3a3b4a63fa5eca
https://doi.org/10.1002/chin.199315282
https://doi.org/10.1002/chin.199315282
Autor:
Borbála Vermes, Erika Samu, Péter Huszthy, Jerald S. Bradshaw, Reed M. Izatt, Mihály Nógrádi, Gabriella Mezey-Vándor
Publikováno v:
ChemInform. 30
Novel acridino- and phenazino-18-crown-6 ligands 5 and 6 were prepared from acridine-4,5-diol (9) and phenazine-1,9-diol (10) with tetraethylene glycol di-p-tosylate (11) using potassium teri-butoxide as a base in THF. New optically pure dimethyl-sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e718d8502b4cc8b033a514cd810b6e68
https://doi.org/10.1002/chin.199924170
https://doi.org/10.1002/chin.199924170
Autor:
Mária Kajtár-Peredy, László Kametler, Borbála Vermes, György M. Keserü, Gabriella Mezey-Vándor, Mihály Nógrádi
Publikováno v:
Liebigs Annalen der Chemie. 1992:1239-1243
Synthesis of Plagiochins A and B, Macrocyclic Bis(bibenzyl) Ethers from Plagiochila acantophylla Plagiochins A (1) and B (2), macrocyclic bis(bibenzyl) ethers with a 16-membered ring, are synthesized. The key steps are the Pd(0)-catalyzed C—C coupl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a37eba600830b3fa7c41223f997b804
https://doi.org/10.1002/jlac.1992199201206
https://doi.org/10.1002/jlac.1992199201206
Autor:
György M. Keserü, Mihály Nógrádi, Gabriella Mezey-Vándor, Borbála Vermes, Mária Kajtár-Peredy
Publikováno v:
Tetrahedron. 48:913-922
Plagiochins C ( 3 ) and D ( 4 ) were synthesized by convergent schemes. Rings C and B were joined by Ullman ether synthesis, the arylaryl bond between rings A and D was formed by Pd(0)-catalysed coupling of an arylboronic acid (ring D) and a bromo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9eac8defb1ac223f12ec2e3e3c918893
https://doi.org/10.1016/s0040-4020(01)88193-x
https://doi.org/10.1016/s0040-4020(01)88193-x
Publikováno v:
Chemische Berichte. 107:3878-3882
Kupplung von 4′,5,6-Triacetoxy-7-hydroxyflavon (3) mit den entsprechenden Acetohalogen-zuckern ergab das 7-β-D-Glucuronid (Scutellarin, 1), das 7 -β-D-Glucopyranosid (Plantaginin, 6) und das 7-β-Rutinosid (8) des scutellarein (2). – Durch Entm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d172a75d83858b7ce01e55010af6ad04
https://doi.org/10.1002/cber.19741071218
https://doi.org/10.1002/cber.19741071218