Zobrazeno 1 - 6
of 6
pro vyhledávání: '"David Ballweg"'
Autor:
Laura M. Lilley, Sarah Kamper, Michael Caldwell, Zer Keen Chia, David Ballweg, Luke Vistain, Jeffrey Krimmel, Teresa Anne Mills, Keith MacRenaris, Paul Lee, Emily Alexandria Waters, Thomas J. Meade
Publikováno v:
Angewandte Chemie. 132:396-402
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1411ca5df8880d6b174532edca903a7
https://doi.org/10.1002/ange.201909933
https://doi.org/10.1002/ange.201909933
Publikováno v:
Journal of the American Chemical Society. 124:12174-12181
Dipotassio-9-germafluorenyl dianion (3b) was synthesized by reduction of 9,9-dichloro-9-germafluorene (4b) with sodium/potassium alloy in tetrahydrofuran. The X-ray crystal structure of 3b, like that for the analogous silicon compound 3a, shows C-C b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f40142765bd213fa603325e5945b8d5
https://doi.org/10.1021/ja020267t
https://doi.org/10.1021/ja020267t
Publikováno v:
Silicon Chemistry. 1:55-58
The reaction of spirobisilafluorene (1) with lithium in dimethoxyethane produces lithium 1-methyl-spirobisilafluorenide (2), a stable pentacoordinate silicon compound with five carbon ligands, and lithium 2-methoxyethoxide, which was identified by tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20b5d092558d8189f41539562c81f503
https://doi.org/10.1023/a:1016012607493
https://doi.org/10.1023/a:1016012607493
Publikováno v:
Journal of the American Chemical Society. 124:49-57
1-Silafluorene dianion was synthesized by potassium reduction of 1,1-dichloro-1-silafluorene in refluxing THF. The X-ray structure of 1,1-dipotassio-1-silafluorene (3b) shows C-C bond length equalization in the five-membered silole ring and C-C bond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a72a18eb7267029b3076e1235ca457bc
https://doi.org/10.1021/ja011821m
https://doi.org/10.1021/ja011821m
Publikováno v:
ChemInform. 33
Reductive coupling of aryl aldehydes and ketones is induced by silole and germole dianions at −78 °C in THF, and 1,2-diols are obtained as the only or major products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aac663f2c8390ba6444d4381ba2825ee
https://doi.org/10.1002/chin.200220068
https://doi.org/10.1002/chin.200220068
Publikováno v:
Organometallics. 20:5769-5770
Reductive coupling of aryl aldehydes and ketones is induced by silole and germole dianions at −78 °C in THF, and 1,2-diols are obtained as the only or major products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00494097a3c9e7f778b1bb0e146f3ba8
https://doi.org/10.1021/om0106837
https://doi.org/10.1021/om0106837