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Merck
CN
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文件

904961

Sigma-Aldrich

Feng L3-PrPr2

≥95%

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别名:
(2S,2′S)-1,1′-(propane-1,3-diyl)bis(2-((2,6-diisopropylphenyl)carbamoyl)pyrrolidine 1-oxide)
经验公式（希尔记法）:
C37H56N4O4
CAS号:
945564-85-2
分子量:
620.86
UNSPSC代码:
12352300
NACRES:
NA.22

检测方案

≥95%

形式

powder

mp

154-159 °C

储存温度

2-8°C

相关类别

应用

L3-PrPr2 is a chiral N,N-dioxide ligand developed by the Feng group. In conjunction with a variety of metal salts, this versatile ligand forms and active catalysts complex with application in many different reactions.

其他说明

Enantioselective Allylation of Ketones Catalyzed by N,N′-Dioxide and Indium(III) Complex

Asymmetric Dearomatization of Indoles through a Michael/Friedel-Crafts-Type Cascade To Construct Polycyclic Spiroindolines

相关产品

产品编号
说明
价格

904988

Feng L3-PiPr2

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

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Xin Zhang et al.
The Journal of organic chemistry, 72(14), 5227-5233 (2007-06-15)
Complexes of (S)-pipecolic acid-, L-proline-, and other amino acid-derived N,N'-dioxides coordinated with different metal ions have been investigated in the enantioselective allylation of ketones. A variety of aromatic ketones were found to be suitable substrates in the presence of the
Xiaohu Zhao et al.
Angewandte Chemie (International ed. in English), 54(13), 4032-4035 (2015-02-05)
A highly efficient asymmetric dearomatization of indoles was realized through a cascade reaction between 2-isocyanoethylindole and alkylidene malonates catalyzed by a chiral N,N'-dioxide/Mg(II) catalyst. Fused polycyclic indolines containing three stereocenters were afforded in good yields with excellent diastereo- and enantioselectivities
Hang Zhang et al.
Chemical communications (Cambridge, England), 54(88), 12511-12514 (2018-10-23)
The catalytic asymmetric ene-type reactions of vinylogous hydrazone were accomplished by using chiral N,N'-dioxide-metal salt complexes as catalysts. A wide range of electrophiles, including isatins, α-ketoester, imines, and aldehydes reacted with (E)-2-methyl-N-(piperidin-1-yl)prop-2-en-1-imine efficiently, affording the corresponding homoallylic alcohols and amines

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