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表单
solid
质量水平
组成
, 4-6 wt. % (loading of catalyst)
反应适用性
reagent type: catalyst
core: ruthenium
reaction type: Ring-Opening Polymerization
SMILES字符串
Cl[Ru](C1N(C2=CC=CC=C2C)CCN1C3=CC=CC=C3C)(O4C(C)C)(Cl)=CC5=C4C=CC=C5
InChI
1S/C17H19N2.C10H12O.2ClH.Ru/c1-14-7-3-5-9-16(14)18-11-12-19(13-18)17-10-6-4-8-15(17)2;1-8(2)11-10-7-5-4-6-9(10)3;;;/h3-10,13H,11-12H2,1-2H3;3-8H,1-2H3;2*1H;/q;;;;+2/p-2
InChI key
AFQRYTARHOMPFY-UHFFFAOYSA-L
一般描述
Less sterically hindered analog of Hoveyda-Grubbs Catalyst® 2nd Generation. Excels at ring-closing metathesis reactions of sterically encumbered olefins. Also useful for the cross metathesis of olefins bearing large allylic substituents. ChemBeads are chemical coated glass beads. ChemBeads offer improved flowability and chemical uniformity perfect for automated solid dispensing and high-throughput experimentation. The method of creating ChemBeads uses no other chemicals or surfactants allowing the user to accurately dispense sub-milligram amounts of chemical.
法律信息
Grubbs Catalyst is a registered trademark of Umicore AG & Co. KG
相关产品
储存分类代码
13 - Non Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
David E White et al.
Journal of the American Chemical Society, 130(3), 810-811 (2008-01-01)
Described in this report is the first total synthesis of elatol, a halogenated sesquiterpene in the chamigrene natural product family. The key disconnections in our synthetic approach include an enantioselective decarboxylative allylation to form the all-carbon quaternary stereocenter and a
Ian C Stewart et al.
Organic letters, 9(8), 1589-1592 (2007-03-24)
[reaction: see text] A series of ruthenium-based metathesis catalysts with N-heterocyclic carbene (NHC) ligands have been prepared in which the N-aryl groups have been changed from mesityl to mono-ortho-substituted phenyl (e.g., tolyl). These new catalysts offer an exceptional increase in
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