Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Yu Mi Chang"'
Publikováno v:
Bulletin of the Korean Chemical Society. 32:2139-2142
Department of Chemistry, Faculty of Science, Gakushuin University, Tokyo 171-8588, JapanReceived October 8, 2010, Accepted April 28, 2011Key Words : Boron neutron capture therapy (BNCT), ortho-carborane, 4-Aminobenzoic acid, 4-Hydroxyben-zoic acid, G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::063e4978ad31aa451ec9e71c99a76414
https://doi.org/10.5012/bkcs.2011.32.6.2139
https://doi.org/10.5012/bkcs.2011.32.6.2139
Publikováno v:
Optical Materials. 30:662-668
Photopolymer compositions for holographic recording were prepared from aromatic diacrylate having phosphine oxide backbone, a hybrid sol–gel, and photoinitiator. The physical and holographic properties of photopolymer were controlled by the ratio o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7b6fc1e23b4242ba21395f27132223a
https://doi.org/10.1016/j.optmat.2007.02.050
https://doi.org/10.1016/j.optmat.2007.02.050
Publikováno v:
Tetrahedron Letters. 46:3053-3056
Petasis reactions of activated forms of quinolines and isoquinolines with electron sufficient boronic acids such as 2-benzofuranboronic acid, trans-2-phenylvinylboronic acid etc in DCM proceeded smoothly at room temperature to provide the correspondi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b5d3060f7b0c8bf4c4a6bf317cc105b
https://doi.org/10.1016/j.tetlet.2005.03.008
https://doi.org/10.1016/j.tetlet.2005.03.008
Publikováno v:
Tetrahedron Letters. 45:9049-9052
EEDQ and EEDI generated in situ by the reaction of quinoline and isoquinoline with diethyl pyrocarbonate was treated with alkylating reagents having an activated carbon such as diethyl malonate, ethyl acetoacetate etc. in the presence of 0.5 equiv of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::346343b14ca757654e76d13a4bfb214f
https://doi.org/10.1016/j.tetlet.2004.10.032
https://doi.org/10.1016/j.tetlet.2004.10.032
Publikováno v:
Tetrahedron. 59:10331-10338
Reductive alkylation and reductive methylation of aromatic primary amines with carbonyls and 37% formaldehyde using decaborane in one-pot way gave the corresponding tertiary amines in high yields. The reaction condition was extended for the reduction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44cddd034e07df77bddd262b640c544f
https://doi.org/10.1016/j.tet.2003.09.054
https://doi.org/10.1016/j.tet.2003.09.054
Publikováno v:
Bulletin of the Korean Chemical Society. 25:1723-1725
Excess amount of sodium iodide in the absence ofany other additives or along with other carbonyl activatingadditive such as sulfuric acid, chlorotrimethylsilane havebeen employed for the reduction of α-haloketones. Recently,stoichiometric amount of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d18afc2db3d9d5940944ca78db54db59
https://doi.org/10.5012/bkcs.2004.25.11.1723
https://doi.org/10.5012/bkcs.2004.25.11.1723
Autor:
Yu Mi Chang, Hakjune Rhee, Byung Woo Yoo, Min Young Cho, Seung Hwan Lee, Sang Ho Lee, Cheol Min Yoon
Publikováno v:
ChemInform. 36
Homocoupling of aryl iodides and bromides using catalytic amounts of palladium and stoichiometric amounts of indium proceeded smoothly to afford the corresponding biaryls in good to high yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::163422088c11dc140c5c1d837029757b
https://doi.org/10.1002/chin.200546086
https://doi.org/10.1002/chin.200546086
Publikováno v:
ChemInform. 36
Excess amount of sodium iodide in the absence ofany other additives or along with other carbonyl activatingadditive such as sulfuric acid, chlorotrimethylsilane havebeen employed for the reduction of α-haloketones. Recently,stoichiometric amount of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28f09ff766fb43494ce96d3d7491934f
https://doi.org/10.1002/chin.200514051
https://doi.org/10.1002/chin.200514051
Publikováno v:
ChemInform. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c7a05ba0d26120f2b36fab3e6c21340
https://doi.org/10.1002/chin.200412087
https://doi.org/10.1002/chin.200412087
Publikováno v:
ChemInform. 34
Azides were converted to the corresponding carbamates using a system of 20 mol% of decaborane (B10H14) and 20 weight% of 10% Pd/C in methanol in the presence of di-tert-butyl dicarbonate at rt in high yields and to the corresponding amines using a sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dce8843e8818ec283531b368bcc1f851
https://doi.org/10.1002/chin.200307052
https://doi.org/10.1002/chin.200307052