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Merck

682365

Sigma-Aldrich

Grubbs催化剂® M207

Umicore

别名:

二氯[1,3-双(2,4,6-三甲基苯基)-2-咪唑烷亚基](3-甲基-2-亚丁烯基)(三环己基膦)钌(II), Grubbs催化剂® M2b (C827), [SIMes]二氯(3-甲基-2-亚丁烯基)(三环己基膦)Ru(II), 异亚戊烯基(1,3-双(2,4,6-三甲基苯基)-咪唑烷-2-亚基)(三环己基膦)二氯化钌(II)

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About This Item

经验公式(希尔记法):
C44H67Cl2N2PRu
分子量:
826.97
MDL號碼:
分類程式碼代碼:
12161600
PubChem物質ID:
NACRES:
NA.22

反應適用性

core: ruthenium
reagent type: catalyst
reaction type: Olefin Metathesis

儲存溫度

2-8°C

SMILES 字串

C1CCC(CC1)P(C2CCCCC2)C3CCCCC3.C\C(C)=C/C=[Ru](Cl)(Cl)=C4N(CCN4c5c(C)cc(C)cc5C)c6c(C)cc(C)cc6C

InChI

1S/C21H26N2.C18H33P.C5H8.2ClH.Ru/c1-14-9-16(3)20(17(4)10-14)22-7-8-23(13-22)21-18(5)11-15(2)12-19(21)6;1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;1-4-5(2)3;;;/h9-12H,7-8H2,1-6H3;16-18H,1-15H2;1,4H,2-3H3;2*1H;/q;;;;;+2/p-2

InChI 密鑰

LCOFYVWULBZOTA-UHFFFAOYSA-L

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相关类别

應用

一种通用烯烃复分解催化剂,其反应活性与2nd代格拉布斯催化剂®相似。

法律資訊

Umicore产品

产品许可证
该产品及其制造或使用受Umicore PMC拥有或控制的一项或多项已发布或正在申请的美国专利(和国外等同专利)权限管辖。通过Sigma-Aldrich、其关联公司或其授权分销商从Umicore PMC购买此产品,购买者将享受有限的一次性、非排他、不可转让、不可分配的许可。购买者使用此产品可能会侵犯第三方拥有或控制的专利。购买者应自行确保其使用产品未侵犯第三方专利权或超出本协议授予的许可范围。

有关产品的更多信息,请询当地Umicore PMC联系人,网址http://www.pmc.umicore.com。
Grubbs Catalyst is a registered trademark of Umicore AG & Co. KG

象形圖

Flame

訊號詞

Warning

危險聲明

危險分類

Flam. Sol. 2

儲存類別代碼

4.1B - Flammable solid hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Ryan P Murelli et al.
Organic letters, 9(9), 1749-1752 (2007-04-03)
[reaction: see text] In the presence of ruthenium-based olefin metathesis catalysts and triphenylphosphine, alpha,beta-unsaturated aldehydes can be olefinated with diazoacetates. This ruthenium-catalyzed transformation has been employed in tandem with olefin cross-metathesis to convert terminal olefins into 1,3-dienoic esters in a
Kevin M Kuhn et al.
Organic letters, 12(5), 984-987 (2010-02-10)
A series of ruthenium catalysts have been screened under ring-closing metathesis (RCM) conditions to produce five-, six-, and seven-membered carbamate-protected cyclic amines. Many of these catalysts demonstrated excellent RCM activity and yields with as low as 500 ppm catalyst loadings.
A K Chatterjee et al.
Organic letters, 1(11), 1751-1753 (2000-06-03)
[formula: see text] Trisubstituted alkenes have been prepared for the first time via intermolecular olefin cross-metathesis, using 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene ruthenium alkylidene complexes 3a,b in good yields with moderate E selectivity. In addition, protected alcohols near the geminal disubstituted olefin improve reactivity
Schrodi, Y.; Pederson, R.L.
Aldrichimica Acta, 40, 45-45 (2007)
T M Trnka et al.
Accounts of chemical research, 34(1), 18-29 (2001-02-15)
In recent years, the olefin metathesis reaction has attracted widespread attention as a versatile carbon-carbon bond-forming method. Many new applications have become possible because of major advances in catalyst design. State-of-the-art ruthenium catalysts are not only highly active but also

相关内容

Research in the Grubbs group has centered on the development and application of a suite of highly active, selective, and bench stable ruthenium alkylidene complexes capable of catalyzing versatile olefin metatheses.

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