Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Ashkan Fardost"'
Publikováno v:
Advanced Synthesis & Catalysis. 356:870-878
Despite the recent emergence of decarboxylative CC bond forming reactions, methodologies providing internally arylated electron-rich olefins are still lacking. We herein report on palladium(II)-cat ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad783dc769401d3e5a9db3051e3c3411
https://doi.org/10.1002/adsc.201301004
https://doi.org/10.1002/adsc.201301004
Publikováno v:
Comprehensive Organic Chemistry Experiments for the Laboratory Classroom ISBN: 9781849739634
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::331ce9152a94a203a31d02e6541bb3ed
https://doi.org/10.1039/9781849739634-00581
https://doi.org/10.1039/9781849739634-00581
Publikováno v:
Comprehensive Organic Chemistry Experiments for the Laboratory Classroom ISBN: 9781849739634
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e48b154cfa08c98f40bc6679238791a0
https://doi.org/10.1039/9781849739634-00573
https://doi.org/10.1039/9781849739634-00573
Autor:
Francesco Russo, Per Öhrngren, Mats Larhed, Magnus Fagrell, Jon-Sverre Schanche, Ashkan Fardost
Publikováno v:
Organic Process Research & Development. 16:1053-1063
The concept of a nonresonant microwave applicator for continuous-flow organic chemistry is introduced and evaluated. The frequency of the incident microwave radiation can be adjusted between 2.4 and 2.5 GHz to optimize the energy absorbance. The temp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1415a489f84556bb294db84515df4f96
https://doi.org/10.1021/op300003b
https://doi.org/10.1021/op300003b
Publikováno v:
The Journal of Organic Chemistry. 76:2433-2438
A palladium(II)-catalyzed Heck-Mizoroki/Suzuki-Miyaura domino reaction involving metal coordinating dimethylaminoethyl vinyl ethers and a number of electron-rich and electron-deficient arylboronic acids has been developed. Through variation of the te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12a9907776d2079c847873a862379b8a
https://doi.org/10.1021/jo1018188
https://doi.org/10.1021/jo1018188
Publikováno v:
ChemInform. 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ad380d45534d50898e1e93de8381b71
https://doi.org/10.1002/chin.201434062
https://doi.org/10.1002/chin.201434062
Publikováno v:
Tetrahedron Letters. 51:2470-2472
Palladium catalysis was used in Stille-type carbonylative cross-couplings employing Mo(CO)6 as the carbon monoxide source. Robust and convenient transformations were carried out in closed vessels at 100 °C, providing a set of diaryl ketones in good
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42355d309a512dd50123e6a7209bf59f
https://doi.org/10.1016/j.tetlet.2010.02.165
https://doi.org/10.1016/j.tetlet.2010.02.165
Publikováno v:
ChemInform. 42
The treatment of vinyl ethers (I) and (IV) with various arylboronic acids and vinylboronic acid (IIj) in the presence of benzoquinone allows formation of a number of 1,2-difunctionalized ethers.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3bbbe09ba586888532e743e77b13d07
https://doi.org/10.1002/chin.201130084
https://doi.org/10.1002/chin.201130084
Publikováno v:
ChemInform. 41
A mild and novel palladium(II)-catalyzed domino Heck/Suzuki α,β-diarylation-reduction of a dimethylaminoethyl substituted chelating vinyl ether was developed by using electron-rich arylboronic acids in combination with p-benzoquinone. Based on the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a02e542d99bac20a75dd53e1aa770cd
https://doi.org/10.1002/chin.201017045
https://doi.org/10.1002/chin.201017045
Publikováno v:
Chemical Communications. :7587
A mild and novel palladium(II)-catalyzed domino Heck/Suzuki alpha,beta-diarylation-reduction of a dimethylaminoethyl substituted chelating vinyl ether was developed by using electron-rich arylboronic acids in combination with p-benzoquinone. Based on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::391eceab88c7d4cc76448a549c5a1b6b
https://doi.org/10.1039/b918358b
https://doi.org/10.1039/b918358b