Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Kimberly A. Seibert"'
Autor:
Khalil A. Abboud, Marie E. Krafft, Kimberly A. Seibert, James A. Wright, John W. Cran, Chitaru Hirosawa, Thomas F. N. Haxell
Publikováno v:
Tetrahedron. 67:9922-9943
From the initial development of a homologous Morita–Baylis–Hillman reaction utilizing epoxides as electrophiles, the method was expanded to enable the exclusively organocatalyzed intramolecular allylation of enones and to develop the intramolecul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c11f896be736e6be975af36d46fed84e
https://doi.org/10.1016/j.tet.2011.09.061
https://doi.org/10.1016/j.tet.2011.09.061
Publikováno v:
Synlett. 2010:2583-2588
The Morita―Baylis―Hillman alkylation reaction with unsaturated thioesters is described. Five- and six-membered rings are formed with ease and in excellent yields. The method is high yielding with either stoichiometric or catalytic amounts of trib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b4f14dad2ff896c33c0718f58233642
https://doi.org/10.1055/s-0030-1258777
https://doi.org/10.1055/s-0030-1258777
Publikováno v:
Organic Letters. 11:5646-5648
Treatment of diethoxycarbonyl hydrazine derivatives with methyl bromoacetate/Cs(2)CO(3)/MeCN at 50 degrees C followed by heating to 80 degrees C resulted in N-N' bond cleavage to the corresponding carbamates.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a966ddaf637cab193d3f0e4f9bf4db96
https://doi.org/10.1021/ol902313v
https://doi.org/10.1021/ol902313v
Autor:
Kimberly A. Seibert, Marie E. Krafft
Publikováno v:
Synlett. 2006:3334-3336
Using a catalytic amount oftrialkylphosphines, alkyl halides undergo efficient intramolecular Morita-Baylis-Hillman cyclization.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f8ce62790f1906bfa283eb4e899e508
https://doi.org/10.1055/s-2006-951531
https://doi.org/10.1055/s-2006-951531
Publikováno v:
ChemInform. 42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd3d87f60354c9181609e6ee0d6d2002
https://doi.org/10.1002/chin.201109029
https://doi.org/10.1002/chin.201109029
Publikováno v:
ChemInform. 41
Treatment of diethoxycarbonyl hydrazine derivatives with methyl bromoacetate/Cs(2)CO(3)/MeCN at 50 degrees C followed by heating to 80 degrees C resulted in N-N' bond cleavage to the corresponding carbamates.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ef37cec7c980da220948c7de5cfa113
https://doi.org/10.1002/chin.201019052
https://doi.org/10.1002/chin.201019052
Autor:
Kimberly A. Seibert, Marie E. Krafft
Publikováno v:
ChemInform. 38
Using a catalytic amount oftrialkylphosphines, alkyl halides undergo efficient intramolecular Morita-Baylis-Hillman cyclization.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48564d51e6a6978e5465462a54808c98
https://doi.org/10.1002/chin.200715059
https://doi.org/10.1002/chin.200715059
Publikováno v:
Journal of the American Chemical Society. 128:4174-4175
An intermediate phosphonium salt has never been isolated from the Morita-Baylis-Hillman (MBH) reaction. Due to the weakly basic counterion produced in the MBH alkylation and allylation reactions, the reaction can be stopped after electrophilic attack
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76bb9de2fa5aeb8e7bef91661699b794
https://doi.org/10.1021/ja057595o
https://doi.org/10.1021/ja057595o
Publikováno v:
Chemical Communications. :5772
sp3 Hybridized electrophiles, never before used in the organomediated Morita–Baylis–Hillman reaction, now facilitate the formation of five- and six-membered enone cycloalkylation products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0430d2cae7398b9884513fb1a781a636
https://doi.org/10.1039/b512665g
https://doi.org/10.1039/b512665g
Publikováno v:
Chemical Communications; Nov2005, Vol. 2005 Issue 46, p5772-5774, 3p