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(R)-2,4-DIMETHYL-3,4-DIHYDRO-3-PIPERIDINYL-DINAPHTHO-[2,1-D:1',2'-F]-1H-[1,3,2]-DIAZAPHOSPHEPINE-3-OXIDE

Compound with spectra: 4 NMR

(R)-2,4-DIMETHYL-3,4-DIHYDRO-3-PIPERIDINYL-DINAPHTHO-[2,1-D:1',2'-F]-1H-[1,3,2]-DIAZAPHOSPHEPINE-3-OXIDE
SpectraBase Compound ID 2WQH6VY4onK
InChI InChI=1S/C27H28N3OP/c1-28-24-16-14-20-10-4-6-12-22(20)26(24)27-23-13-7-5-11-21(23)15-17-25(27)29(2)32(28,31)30-18-8-3-9-19-30/h4-7,10-17H,3,8-9,18-19H2,1-2H3
InChIKey IQRFUEOOIOHMST-UHFFFAOYSA-N
Mol Weight 441.51 g/mol
Molecular Formula C27H28N3OP
Exact Mass 441.197 g/mol

View Spectrum of (R)-2,4-DIMETHYL-3,4-DIHYDRO-3-PIPERIDINYL-DINAPHTHO-[2,1-D:1',2'-F]-1H-[1,3,2]-DIAZAPHOSPHEPINE-3-OXIDE

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (R)-2,4-DIMETHYL-3,4-DIHYDRO-3-PIPERIDINYL-DINAPHTHO-[2,1-D:1',2'-F]-1H-[1,3,2]-DIAZAPHOSPHEPINE-3-OXIDE

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (R)-2,4-DIMETHYL-3,4-DIHYDRO-3-PIPERIDINYL-DINAPHTHO-[2,1-D:1',2'-F]-1H-[1,3,2]-DIAZAPHOSPHEPINE-3-OXIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (R)-2,4-DIMETHYL-3,4-DIHYDRO-3-PIPERIDINYL-DINAPHTHO-[2,1-D:1',2'-F]-1H-[1,3,2]-DIAZAPHOSPHEPINE-3-OXIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (R)-(-)-2,4-DIMETHYL-3,4-DIHYDRO-3-PIPERIDINYL-DINAPHTHO-[2,1-D:1',2'-F]-1H-[1,3,2]-DIAZA-PHOSPHEPINE-3-OXIDE
(R,R)-N,N'-BIS-[4,5-DIHYDRO-3,5-DIMETHYL-4-(3H-DINAPHTHO-[2,1-D:1',2'-F]-[1,3,2]-2-OXODIAZAPHOSPHEPINO)]-N,N'-DIMETHYL-1,6-HEXANEDIAMINE
(R,R)-N,N'-BIS-[4,5-DIHYDRO-3,5-DIMETHYL-4-(3H-DINAPHTHO-[2,1-D:1',2'-F]-[1,3,2]-2-OXODIAZAPHOSPHEPINO)]-N,N'-DIMETHYL-1,5-PENTANEDIAMINE
BLGLTZMTDBOUAG-UHFFFAOYSA-N
(R,R)-N,N'-BIS-[4,5-DIHYDRO-3,5-DIMETHYL-4-(3H-DINAPHTHO-[2,1-D:1',2'-F]-[1,3,2]-2-OXODIAZAPHOSPHEPINO)]-N,N'-DIMETHYL-1,4-BUTANEDIAMINE
(R,R)-N,N'-BIS-[4,5-DIHYDRO-3,5-DIMETHYL-4-(3H-DINAPHTHO-[2,1-D:1',2'-F]-[1,3,2]-2-OXODIAZAPHOSPHEPINO)]-N,N'-DIMETHYL-1,3-PROPANEDIAMINE
(S)-4-(Diisobutylamino)-3,5-dimethyl-4,5-dihydro-3H-dinaphtho[2,1-d:1',2'-f][1,3,2]diazaphosphepine-4-selenide
(11bR)-4-(Pyrrolidin-1-yl)-3,5-di-p-tolyl-3,5-dihydro-4H-dinaphtho[2,1-d:1',2'-f][1,3,2]diazaphosphepine
4-[(2-Isopropyl-5-methylcyclohexyl)oxy]-3,5-dimethyl-4,5-dihydro-3H-dinaphtho[2,1-d:1,2-f][1,3,2]diazaphosphepine
(R)-(-)-2-(Dimethylamino)-2'-(diphenylphosphinoyl)-1,1'-binaphthyl
2-(TERT.-BUTYLPHENYLPHOSPHINO)-2'-N,N-DIMETHYLAMINO-1,1'-BINAPHTHYL
Title Journal or Book Year
Synthesis of Phosphoramides for the Lewis Base-Catalyzed Allylation and Aldol Addition Reactions The Journal of Organic Chemistry 1999
Chemistry of Trichlorosilyl Enolates. 1. New Reagents for Catalytic, Asymmetric Aldol Additions Journal of the American Chemical Society 1996
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