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Merck

795682

Sigma-Aldrich

(4R,4′R,5S,5′S)-2,2′-(1-Methylethylidene

95%

别名:

2,2-Bis[2-(4R,5S-diphenyl-1,3-oxazolinyl)]propane

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About This Item

经验公式(希尔记法):
C33H30N2O2
分子量:
486.60
MDL號碼:
分類程式碼代碼:
12352005
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

95%

形狀

solid

mp

164-169 °C

官能基

ether
phenyl

SMILES 字串

CC(C1=N[C@H](C2=CC=CC=C2)[C@H](C3=CC=CC=C3)O1)(C)C4=N[C@H](C5=CC=CC=C5)[C@H](C6=CC=CC=C6)O4

InChI

1S/C33H30N2O2/c1-33(2,31-34-27(23-15-7-3-8-16-23)29(36-31)25-19-11-5-12-20-25)32-35-28(24-17-9-4-10-18-24)30(37-32)26-21-13-6-14-22-26/h3-22,27-30H,1-2H3/t27-,28-,29+,30+/m1/s1

InChI 密鑰

ZWWGNCSTEMMQOQ-XAZDILKDSA-N

應用

(4R,4′R,5S,5′S)-2,2′-(1-Methylethylidene) or (4S,5R)-Bis-Phbox) can be used as a ligand:
  • To prepare selective exo-catalysts for enantioselective 1,3-dipolar cycloaddition reactions.
  • In the asymmetric aminooxygenation of alkenes in the presence of tetramethylaminopyridyl radical (TEMPO) as an oxidant and copper(II) triflate as a catalyst.
  • In asymmetric aminofluorination of olefins using an iron catalyst.

This chiral Box ligand was most recently shown to mediate an asymmetric aminofluorination of olefins utlizing Xtalfuor-E (719439) and TREAT-HF (344648). The resulting cyclic carbamates can be readily converted into their concomitant beta-fluoro amino acids.

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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分析证书(COA)

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Copper catalyzed enantioselective intramolecular aminooxygenation of alkenes
Fuller PH, et al.
Journal of the American Chemical Society, 130(52), 17638-17639 (2008)

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