Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Frederic Ballaschk"'
Autor:
Frederic Ballaschk, Stefan F. Kirsch
Publikováno v:
Iodine Catalysis in Organic Synthesis. :299-334
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70a0b552a2bb9673be7a2c238eb66993
https://doi.org/10.1002/9783527829569.ch11
https://doi.org/10.1002/9783527829569.ch11
Publikováno v:
European Journal of Organic Chemistry. 2020:6078-6080
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48d32fe67d3df73e00c00794eb32bf3d
https://doi.org/10.1002/ejoc.202001046
https://doi.org/10.1002/ejoc.202001046
Autor:
Frederic Ballaschk, Marcel Jaschinski, Adrián Gómez-Suárez, Yasemin Özkaya, Francisco José Aguilar Troyano
Publikováno v:
Chemistry – A European Journal. 25:14054-14058
The synthesis of tertiary alkyl fluorides through a formal radical deoxyfluorination process is described herein. This light-mediated, catalyst-free methodology is fast and broadly applicable allowing for the preparation of C-F bonds from (hetero)ben
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f42732c48cbb880a5e1935fa37515f9
https://doi.org/10.1002/chem.201903702
https://doi.org/10.1002/chem.201903702
Autor:
Stefan F. Kirsch, Frederic Ballaschk
Publikováno v:
Green Chemistry. 21:5896-5903
It is shown how secondary alcohols are oxidized to provide the corresponding ketones by use of Oxone® and solid-supported hypervalent iodine catalysts. Under experimentally simple conditions with acetonitrile at elevated temperatures, excellent conv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10f38daa9f1e6d772859cd1becadcc5d
https://doi.org/10.1039/c9gc02605c
https://doi.org/10.1039/c9gc02605c
Publikováno v:
Synthesis. 49:3107-3111
A short and practical synthesis of a new chiral dipyrrolidine is presented. The three-step route includes a hydrogenation and a resolution with mandelic acid, which easily affords large quantities of the title compound.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b4841b26b12f575c3f1d438defbee14
https://doi.org/10.1055/s-0036-1589023
https://doi.org/10.1055/s-0036-1589023
Publikováno v:
RSC Advances. 7:55594-55597
The synthesis of pyrazines is described using a sequence that begins with the diazidation of N-allyl malonamides followed by thermal or copper-mediated cyclization. The pyrazine products possess an ester and a hydroxy group at 2- and 3-positions of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cacb4fc71d6d1022e0fcfd240137fe4
https://doi.org/10.1039/c7ra11529f
https://doi.org/10.1039/c7ra11529f
Autor:
Francisco José, Aguilar Troyano, Frederic, Ballaschk, Marcel, Jaschinski, Yasemin, Özkaya, Adrián, Gómez-Suárez
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
The synthesis of tertiary alkyl fluorides through a formal radical deoxyfluorination process is described herein. This light‐mediated, catalyst‐free methodology is fast and broadly applicable allowing for the preparation of C−F bonds from (hete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ac8f83c5f714a3c391521b05cff92626
https://pubmed.ncbi.nlm.nih.gov/31452265
https://pubmed.ncbi.nlm.nih.gov/31452265