Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Paul D. Weipert"'
Autor:
M. W. Rathke, Paul D. Weipert
Publikováno v:
ChemInform. 23
Symmetrical dimethylsilyl bis-enol ethers are obtained in good yield by reaction of ketones with dichlorodimethylsilane in the presence of triethylamine and sodium iodide. Reaction of ketones with N, N - diethylaminodimethylchlorosilane in the presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::baa1f711ca141136cbfb434cd4659629
https://doi.org/10.1002/chin.199208245
https://doi.org/10.1002/chin.199208245
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c119257e8c4955fb0e2380f48f3fda50
https://doi.org/10.1002/chin.199218265
https://doi.org/10.1002/chin.199218265
Publikováno v:
Journal of the American Chemical Society. 113:9820-9824
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efff09b0eceaabf148457acc0084c6ec
https://doi.org/10.1021/ja00026a016
https://doi.org/10.1021/ja00026a016
Autor:
Paul D. Weipert, M. W. Rathke
Publikováno v:
Synthetic Communications. 21:1337-1351
Symmetrical dimethylsilyl bis-enol ethers are obtained in good yield by reaction of ketones with dichlorodimethylsilane in the presence of triethylamine and sodium iodide. Reaction of ketones with N, N - diethylaminodimethylchlorosilane in the presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::667f65ae82bed3266a2f872c644490f5
https://doi.org/10.1080/00397919108021281
https://doi.org/10.1080/00397919108021281
Autor:
Paul D. Weipert, Michael W. Rathke
The Reformatsky reaction is the reaction of an α-halo ester with an aldehyde or ketone in the presence of zinc metal as shown in Scheme 1. The usual product of the reaction is a (β-hydroxy ester, which may be dehydrated in subsequent steps to give
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64a193b30aa6dd6b4c1d8189fce3a0c4
https://doi.org/10.1016/b978-0-08-052349-1.00030-5
https://doi.org/10.1016/b978-0-08-052349-1.00030-5
