Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Fatma Türkyilmaz"'
Publikováno v:
Journal of Organometallic Chemistry. 847:167-172
Reaction of the strongly electrophilic borane trans -pentenyl-B(C 6 F 5 ) 2 ( 5 ) with TEMPO gave the 2:1 addition product (C 6 F 5 ) 2 B( ONHR 2 ) CH CH CH(ONR 2 )-C 2 H 5 ( 8 ), (NR 2 = tetramethylpiperidinyl). It is thought to be formed by TEMPO a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be9892e776a2da37fe3375cf39e2b5f9
https://doi.org/10.1016/j.jorganchem.2017.03.030
https://doi.org/10.1016/j.jorganchem.2017.03.030
Autor:
Armido Studer, Matthias Tesch, Constantin G. Daniliuc, Fatma Türkyilmaz, Gerald Kehr, Gerhard Erker, Jun Li
Publikováno v:
Angewandte Chemie International Edition. 55:1470-1473
B(C6F5)2-containing boryldienes 4 underwent the addition of two molar equivalents of TEMPO to give N,O-bonded four-membered heterocyclic products 7. The reaction is a metal-free example of the generation of reactive nitrogen-centered TEMPO radical de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::194d9e0e9db71edc95db3e2b35578fd6
https://doi.org/10.1002/anie.201509114
https://doi.org/10.1002/anie.201509114
Autor:
Gerald Kehr, Melanie Siedow, Gerhard Erker, Hellmut Eckert, Constantin G. Daniliuc, Fang Ge, Fatma Türkyilmaz
Publikováno v:
Chemistry - An Asian Journal. 10:2497-2502
Hydroboration of the conjugated enynes 1 a and 1 b with Piers' borane [HB(C6F5)2] gave the respective dienylboranes trans-2 c and trans-2 d. Their photolysis resulted in the formation of the dihydroborole products 3 c and 3 d. Both were converted to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b90f919f30f5bfe140096a8e3b969ba
https://doi.org/10.1002/asia.201500636
https://doi.org/10.1002/asia.201500636
Autor:
Constantin G. Daniliuc, Fatma Türkyilmaz, Stefan Grimme, Gerhard Erker, Christoph Bannwarth, Guo-Qiang Chen, Gerald Kehr
Publikováno v:
Organic & Biomolecular Chemistry. 13:10477-10486
The dienylborane 2a was prepared by regioselective alkyne hydroboration of the conjugated enyne 1a with Piers’ borane [HB(C6F5)2]. Its reaction with a series of acetophenone derived enamines 3 resulted in the formation of the strong enamine β-carb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b735423eef5ba8f8db643d491cb34e6
https://doi.org/10.1039/c5ob01602a
https://doi.org/10.1039/c5ob01602a