Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Trimethylstannane"'
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 61:749-756
Microtubules are a target for a broad spectrum of drugs used as chemotherapeutics to treat hematological malignancies and solid tumors. Most of these drugs have significant dose-limiting toxicities including peripheral neuropathies that can be debili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3af9d6b84a2a1b257cb44829304ef4f3
https://doi.org/10.1002/jlcr.3631
https://doi.org/10.1002/jlcr.3631
Autor:
Ho Cheol Jin, Nadhila Sylvianti, Dong Geun Kim, Doo Kyung Moon, Youn Hwan Kim, Joo Hyun Kim, Ratna Dewi Maduwu
Publikováno v:
Macromolecular Research. 26:552-556
Electron acceptor-donor-acceptor type oligomers based on benzothiadiazole (BT) unit and a (4,8-bis((2-ethylhexyl)oxy)benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl) bis(trimethylstannane) (BDT) unit have been designed and prepared as electron-donating mat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdde988c4220cf4f3ec38eea36637794
https://doi.org/10.1007/s13233-018-6066-4
https://doi.org/10.1007/s13233-018-6066-4
Autor:
Katsuya Tomizawa, Masaichi Saito, Nobuaki Kurokawa, Tomoyuki Tajima, Lucian-Cristian Pop, Hiroaki Ebata
Publikováno v:
European Journal of Inorganic Chemistry. 2017:4969-4975
Group 14 monolithio compounds with sterically encumbered terphenyl ligands, ArM14(SiHMe2)2Li [M14 = Si, Ge, Sn; Ar = 2,6-bis(2,6-diisopropylphenyl)phenyl and 2,6-bis(2,4,6-triisopropylphenyl)phenyl], were prepared by transmetalation reactions of ArM1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d304be954c579c908851d021a3325430
https://doi.org/10.1002/ejic.201700945
https://doi.org/10.1002/ejic.201700945
Autor:
Pu Luo, Joseph P. Dinnocenzo
Publikováno v:
The Journal of organic chemistry. 82(20)
The aryl/methyl fragmentation selectivities for the photooxidations of phenyltrimethylstannane and (4-methylphenyl)trimethylstannane by 1,2,4,5-tetracyanobenzene in acetonitrile were found to depend on the codonor used to generate the stannane cation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::158b35217892292f3392dc773592c64f
https://pubmed.ncbi.nlm.nih.gov/29016139
https://pubmed.ncbi.nlm.nih.gov/29016139
Autor:
Karin Dölling
Publikováno v:
Journal of the Serbian Chemical Society, Vol 77, Iss 7, Pp 873-877 (2012)
Following the Sch?llkopf methodology the reaction of (2S)-2,5- dihydro-3,6-dimethoxy-2-isopropylpyrazine 1 with iodomethyl trimethylstannane gives (2S,5S)-2,5-dihydro-3,6-dimethoxy-5-trimethylstannylmethyl-2- isopropylpyrazine 2 in good yields. The o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e64182d1a0488f7f7504217e1d408740
http://www.doiserbia.nb.rs/img/doi/0352-5139/2012/0352-51391200007D.pdf
http://www.doiserbia.nb.rs/img/doi/0352-5139/2012/0352-51391200007D.pdf
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 45:987-994
The synthesis of two 125I-labeled trisubstituted aromatic melatonergic agents is reported. N-[[2-[125I]iodo-5-methoxyphenyl)-1R, 2R-cyclopropyl]methyl] butanamide was prepared from the corresponding thallium salt and Na 125I in radiochemical yields o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::334384c4fc8aaef75fa87488316b06aa
https://doi.org/10.1002/jlcr.618
https://doi.org/10.1002/jlcr.618
Autor:
Iain Coldham, Richard Hufton
Publikováno v:
Tetrahedron. 52:12541-12552
α-Aminocarbanions, generated by transmetallation of aminomethylstannanes, cyclize onto an unactivated alkene to give 3-alkylpyrrolidines. The intermediate organolithium either reincorporates trimethyltin or, from the tributylstannanes, can be trappe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2183a1f23bfaa815f0f1d9261a8ed82
https://doi.org/10.1016/0040-4020(96)00734-x
https://doi.org/10.1016/0040-4020(96)00734-x
Publikováno v:
Zeitschrift f�r anorganische und allgemeine Chemie. 621:63-71
Zinnverbindungen des Typs Me3SnCH2C(NHCOR)(COOEt)2 (1: R = CH3; 2: R = H) werden durch Umsetzung von Acylaminomalonsaureestern mit Iodomethyltrimethylstannan dargestellt. Die Halogenierung von 1 und 2 liefert die halogenostannylsubstituierten Verbind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59adec4b682d533884eb760d04b92001
https://doi.org/10.1002/zaac.19956210112
https://doi.org/10.1002/zaac.19956210112
Autor:
H. Weichmann, F. Richter
Publikováno v:
Journal of Organometallic Chemistry. 466:77-87
A series of 2,2-difunctional organotin compounds of the general type Me 3 SnCH 2 CHXY (X, Y = P(O)R 2 or C(O)R; R = O i Pr, OEt or Ph) has been synthesized by stannylmethylation of the appropriate 2,2-difunctional methanides NA[CHXY] with iodomethyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca7e128c1284fdbe87f877fd96437eeb
https://doi.org/10.1016/0022-328x(94)88031-x
https://doi.org/10.1016/0022-328x(94)88031-x
Autor:
Viktor O. Iaroshenko, Marcelo Vilches-Herrera, Peter Langer, Dmytro Ostrovskyi, Katharina Vlach, Verena Specowius, Alexander Villinger, Satenik Mkrtchyan
Publikováno v:
ChemInform. 42
Difluoromethyl-containing heteroannulated pyridines, pyrimidines and pyrazoles are prepared by a two step method. The regioselective cyclizations of electron-excessive aminoheterocycles, hydrazines and amidines with CF 2 Cl-substituted 1,3-dicarbonyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3467bcf3bcd447753be265141b492d05
https://doi.org/10.1002/chin.201147139
https://doi.org/10.1002/chin.201147139