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Merck
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重要文件

905348

Sigma-Aldrich

Rh2(R-p-Ph-TPCP)4

同義詞:

Dirhodium tetrakis((S,R)-1-(4-phenyl(phenyl))-2,2-diphenylcyclopropanecarboxylate), Dirhodium tetrakis[(R)-1-(4-phenyl(phenyl))-2,2- diphenylcyclopropane carboxylate], Tetrakis[(R)-1-(4-phenyl(phenyl))-2,2- diphenylcyclopropane carboxylato]dirhodium(II)

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About This Item

經驗公式(希爾表示法):
C112H84O8Rh2
CAS號碼:
分子量::
1763.67
分類程式碼代碼:
12352101
NACRES:
NA.22

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產品號碼
描述
訂價

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Liangbing Fu et al.
Journal of the American Chemical Society, 138(18), 5761-5764 (2016-04-12)
Enantioselective C-H functionalization of relatively electron-deficient methyl sites was achieved with the combination of 2,2,2-trichloroethyl aryldiazoacetates and tetrakis(triarylcyclopropanecarboxylate) dirhodium catalysts. The substrate scope of the transformation was relatively broad, and C-H functionalization products were furnished with excellent levels of enantioselectivity.
Changming Qin et al.
Journal of the American Chemical Society, 136(27), 9792-9796 (2014-06-17)
The influence of sterically demanding dirhodium tetracarboxylate catalysts on the site selectivity of C-H functionalization by means of rhodium carbene-induced C-H insertion is described. The established dirhodium tetraprolinate-catalyzed reactions of aryldiazoacetates cause preferential C-H functionalization of secondary C-H bonds as
Changming Qin et al.
Journal of the American Chemical Society, 135(39), 14516-14519 (2013-09-13)
Rhodium-catalyzed reaction of vinyldiazoacetates with nitrones results in a formal [3+2]-cycloaddition to generate 2,5-dihydroisoxazoles with high levels of asymmetric induction. The cascade reaction begins with a vinylogous addition event, followed by an iminium addition ring-closure/hydride migration/alkene isomerization cascade. Dirhodium tetrakis(triarylcyclopropanecarboxylates)

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