Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Anne Eeg Jensen"'
Publikováno v:
Organic Letters. 4:1819-1822
[reaction: see text] Functionalized Grignard reagents, derived from readily available o-iodoaniline derivatives and obtained via a straightforward iodine-magnesium exchange, can be used to prepare a wide range of polyfunctional indoles, quinolines, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17bbea8c1e831d731ef37d2365ad49b3
https://doi.org/10.1021/ol025597x
https://doi.org/10.1021/ol025597x
Autor:
Wolfgang Dohle, Ioannis Sapountzis, Paul Knochel, Viet Anh Vu, Anne Eeg Jensen, David M. Lindsay
Publikováno v:
Synthesis. 2002:565-569
Functionalized magnesium reagents have been prepared via an iodine-magnesium exchange. These reagents can be either trapped directly with aldehydes or transmetallated to copper or zinc to participate in cross-coupling reactions. The iodine-magnesium
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00f616a0bc97acf9a35d07f0f39db8b7
https://doi.org/10.1055/s-2002-20955
https://doi.org/10.1055/s-2002-20955
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b03ad64c1df1cbcdb92236bee73927ee
https://doi.org/10.1055/s-2001-12323
https://doi.org/10.1055/s-2001-12323
Autor:
Paul Knochel, Anne Eeg Jensen
Publikováno v:
The Journal of Organic Chemistry. 67:79-85
In the presence of Bu(4)NI (3 equiv) and 4-fluorostyrene (20 mol %), unreactive primary and secondary alkylzinc iodides undergo nickel-catalyzed cross-couplings with various primary alkyl iodides or bromides. More reactive secondary dialkylzincs and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce7e6d6d569327e7c097350a933fbeee
https://doi.org/10.1021/jo0105787
https://doi.org/10.1021/jo0105787
Publikováno v:
Tetrahedron. 56:4197-4201
ortho-Substituted aryl iodides and nonaflates undergo nickel-catalyzed cross-coupling reactions with functionalized alkylzinc iodides in the solid-phase as well as in solution providing high HPLC purities and good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49454abd0661967c59bac2b7d00dfffd
https://doi.org/10.1016/s0040-4020(00)00344-6
https://doi.org/10.1016/s0040-4020(00)00344-6
Publikováno v:
Organic Letters. 1:1323-1326
The addition of Bu4NI has been found to accelerate the palladium(0)-catalyzed cross-coupling between benzylic zinc bromides and aryl or alkenyl triflates. Remarkably, it further allows a new nickel(0)-catalyzed cross-coupling between functionalized b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19b46ffe20bf030647119c988b3e03fc
https://doi.org/10.1021/ol9907872
https://doi.org/10.1021/ol9907872
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fe606d4dd51a063f75b9ba3e73be4bc
https://doi.org/10.1002/chin.200004076
https://doi.org/10.1002/chin.200004076
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d788e9ab036cf712b44593b549cf60e9
https://doi.org/10.1002/chin.200129081
https://doi.org/10.1002/chin.200129081
Autor:
Paul Knochel, Anne Eeg Jensen
Publikováno v:
ChemInform. 33
Protected 2-iodo-1,4-phenylenediamines were converted to the corresponding magnesium derivative by performing an iodine–magnesium exchange. After transmetalation with zinc bromide, a palladium(0)-catalyzed cross-coupling with various aryl iodides a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da3dcbafa30edfea07a0ebe734c7655e
https://doi.org/10.1002/chin.200243111
https://doi.org/10.1002/chin.200243111
Publikováno v:
ChemInform. 33
Functionalized Grignard reagents, derived from readily available o-iodoaniline derivatives and obtained via a straightforward iodine−magnesium exchange, can be used to prepare a wide range of polyfunctional indoles, quinolines, and quinazolinones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2727f8ad327df2cc6102668ba4387dc
https://doi.org/10.1002/chin.200242135
https://doi.org/10.1002/chin.200242135