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Merck
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905542

Sigma-Aldrich

(R,R)-SINpEt⋅HBF4

≥95%

别名:

1,3-Bis((R)-1-(naphthalen-1-yl)ethyl)-4,5-dihydro-1H-imidazol-3-ium tetrafluoroborate

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About This Item

经验公式（希尔记法）:
C27H27BF4N2
CAS号:
1344155-18-5
分子量:
466.32
分類程式碼代碼:
12352101
NACRES:
NA.22

應用

(R,R)-SINpEt⋅HBF4 is a chiral NHC ligand developed in the Glorius Lab for use in Ru(II) catalyzed enantioselective hydrogenations. It has been employed for the regioselectivity asymmetric hydrogenation of quinoxalines, benzofurans, thiophenes, indolizines, isocoumarins and many other heterocycles.
Product can be used with our benchtop hydrogen generator, H-Genie Lite (Z744083)

其他說明

Ligand-Controlled Highly Regioselective and Asymmetric Hydrogenation of Quinoxalines Catalyzed by Ruthenium N-Heterocyclic Carbene Complexes

Ruthenium–NHC–Diamine Catalyzed Enantioselective Hydrogenation of Isocoumarins

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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Wei Li et al.
Journal of the American Chemical Society, 139(7), 2585-2588 (2017-02-02)
A novel and practical chiral ruthenium-NHC-diamine system is disclosed for the enantioselective hydrogenation of isocoumarins, which provides a new concept to apply (chiral) NHC ligands in asymmetric catalysis. A variety of optically active 3-substituted 3,4-dihydroisocoumarins were obtained in excellent enantioselectivities
Ligand-controlled highly regioselective and asymmetric hydrogenation of quinoxalines catalyzed by ruthenium N-heterocyclic carbene complexes.
Slawomir Urban et al.
Angewandte Chemie (International ed. in English), 50(16), 3803-3806 (2011-03-29)
Wei Li et al.
Chemical science, 9(29), 6260-6263 (2018-08-10)
An efficient synthesis of optically active 4-substituted 2-oxazolidinones by the ruthenium(ii)-NHC-catalysed asymmetric hydrogenation of 2-oxazolones was developed. Excellent enantioselectivities (up to 96% ee) and yields (up to 99%) were obtained for a variety of substrates, bearing a range of functional

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