Zobrazeno 1 - 10
of 11
pro vyhledávání: '"James W. Grebinski"'
Publikováno v:
CHIMIA, Vol 61, Iss 5 (2007)
We present an array of [4+2] cycloaddition reactions between ketene enolates, catalytically derived from acid chlorides and cinchona alkaloid nucleophilic catalysts in the presence of stoichiometric base, and o-benzoquinone derivatives. These cycload
Externí odkaz:
https://doaj.org/article/9c5bb698a6d84e249460d1f21106a562
Publikováno v:
Chemistry of Materials. 17:4416-4425
The synthesis of narrow diameter (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25c4a3b8911c447fca6b50226d500afd
https://doi.org/10.1021/cm050952+
https://doi.org/10.1021/cm050952+
Publikováno v:
Chemistry of Materials. 16:5260-5272
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f0a99bbf7fd675c1710e0e3c0573f50
https://doi.org/10.1021/cm048498h
https://doi.org/10.1021/cm048498h
Publikováno v:
The Journal of Physical Chemistry B. 108:9745-9751
The synthesis, characterization, and catalytic ability of gold/bismuth (Au/Bi) core/shell nanocrystals for promoting asymmetric 1D nanowire growth is described. A biphasic gold reduction approach i...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b19ae9352629eb14c23560faf663f44
https://doi.org/10.1021/jp0496856
https://doi.org/10.1021/jp0496856
Publikováno v:
ChemInform. 39
We present an array of [4+2] cycloaddition reactions between ketene enolates, catalytically derived from acid chlorides and cinchona alkaloid nucleophilic catalysts in the presence of stoichiometric base, and o-benzoquinone derivatives. These cycload
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a488d222903a48a193a0d53c01505772
https://doi.org/10.1002/chin.200833245
https://doi.org/10.1002/chin.200833245
Publikováno v:
ChemInform. 38
In this Communication, we report a system in which an achiral Lewis acid (activating the diene) works in concert with a chiral nucleophile (dienophile) to effect the first highly enantio- and regioselective catalytic inverse electron demand Diels−A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1e255d32f83ff2d7f42b7f4d56c86b7
https://doi.org/10.1002/chin.200709165
https://doi.org/10.1002/chin.200709165
Publikováno v:
SPIE Proceedings.
The solution phase synthesis of narrow diameter (< 10 nm) CdSe NWs is described. Crystalline NWs with lengths between 1-10 mm are obtained using a seeded solution approach, whereby NW growth is catalyzed by Au/Bi core/shell NPs. A gold biphasic reduc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef57bf4ecf47dd7f0a1c3c72e07ff953
https://doi.org/10.1117/12.557526
https://doi.org/10.1117/12.557526
Publikováno v:
MRS Proceedings. 848
The solution phase synthesis of narrow diameter CdSe and PbSe nanowires (NWs) is described. Crystalline NWs with lengths between 1–10 μm are obtained using a seeded solution approach, whereby NW growth is catalyzed by Au/Bi core/shell nanoparticle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9208bc6bc3535e70f2d72e4d356bf2f
https://doi.org/10.1557/proc-848-ff8.6
https://doi.org/10.1557/proc-848-ff8.6
Publikováno v:
Journal of the American Chemical Society. 128:13370-13371
In this Communication, we report a system in which an achiral Lewis acid (activating the diene) works in concert with a chiral nucleophile (dienophile) to effect the first highly enantio- and regioselective catalytic inverse electron demand Diels−A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69136906e0dd31beba41d73d27b78c5a
https://doi.org/10.1021/ja065754d
https://doi.org/10.1021/ja065754d
Publikováno v:
CHIMIA, Vol 61, Iss 5 (2007)
We present an array of [4+2] cycloaddition reactions between ketene enolates, catalytically derived from acid chlorides and cinchona alkaloid nucleophilic catalysts in the presence of stoichiometric base, and o-benzoquinone derivatives. These cycload
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c548220c36d5a293b9c916b81d2463ea
https://doi.org/10.2533/chimia.2007.240
https://doi.org/10.2533/chimia.2007.240