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905348

Sigma-Aldrich

Rh2(R-p-Ph-TPCP)4

Synonym(s):

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

Empirical Formula (Hill Notation):
C112H84O8Rh2
CAS Number:
1415389-64-8
Molecular Weight:
1763.67
UNSPSC Code:
12352101
NACRES:
NA.22

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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
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.

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