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About This Item
Empirical Formula (Hill Notation):
C88H64Br4O8Rh2
CAS Number:
Molecular Weight:
1774.87
MDL number:
NACRES:
NA.22
UNSPSC Code:
12161600
Product Name
Rh2(R-BTPCP)4,
form
powder or crystals
mp
>300 °C
Application
Rh catalyst developed by the Davies lab used for enantioselective cyclopropanations and C-H funcionalization under low catalyst loadings.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Changming Qin et al.
Organic letters, 15(2), 310-313 (2013-01-05)
The rhodium-catalyzed reaction of 2-diazo-5-arylpent-4-enoates can be controlled by the appropriate choice of catalyst and catalyst loading to form either 2-arylbicyclo[1.1.0]butane carboxylates or cyclohexene derivatives. Both products are produced in a highly diastereoselective manner, with 2-arylbicyclo[1.1.0]butane carboxylates preferentially formed under
Ji-Min Yang et al.
Journal of the American Chemical Society, 139(10), 3784-3789 (2017-02-15)
Herein, we report transition-metal-catalyzed B-H bond insertion reactions between borane adducts and alkynes to afford organoboron compounds in excellent yields under mild reaction conditions. This successful use of alkynes as carbene precursors in these reactions constitutes a new route to
Daniel Rackl et al.
Organic letters, 19(12), 3055-3058 (2017-06-06)
A tandem reaction system has been developed for the preparation of donor/acceptor-substituted diazo compounds in continuous flow coupled to dirhodium-catalyzed C-H functionalization or cyclopropanation. Hydrazones were oxidized in flow by solid-supported N-iodo-p-toluenesulfonamide potassium salt (PS-SO2NIK) to generate the diazo compounds