904988
Feng L3-PiPr2
Sinónimos:
(2S,2′S)-1,1′-(propane-1,3-diyl)bis(2-((2,6-diisopropylphenyl)carbamoyl)piperidine-1-oxide)
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About This Item
Fórmula empírica (notación de Hill):
C39H60N4O4
Número de CAS:
Peso molecular:
648.92
UNSPSC Code:
12352300
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form
solid
storage temp.
2-8°C
Application
L3-PiPr2 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.
Other Notes
An N,N′-Dioxide/In(OTf)3 Catalyst for the Asymmetric Hetero-Diels–Alder Reaction Between Danishefsky′s Dienes and Aldehydes: Application in the Total Synthesis of Triketide
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
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
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Referencia del producto
Descripción
Precios
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificados de análisis (COA)
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An N,N'-dioxide/In(OTf)3 catalyst for the asymmetric Hetero-Diels-Alder reaction between Danishefsky's dienes and aldehydes: application in the total synthesis of triketide.
Zhipeng Yu et al.
Angewandte Chemie (International ed. in English), 47(7), 1308-1311 (2008-01-08)
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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