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(2,2-DIMETHYL-4,4,8,8-TETRAPHENYL-TETRAHYDRO-[1,3]-DIOXOLO-[4,5-E]-[1,3,2]-DIOXAPHOSPHEPIN-6-YL)-(1-PHENYL-ETHYL)-AMINE

Compound with spectra: 2 NMR

(2,2-DIMETHYL-4,4,8,8-TETRAPHENYL-TETRAHYDRO-[1,3]-DIOXOLO-[4,5-E]-[1,3,2]-DIOXAPHOSPHEPIN-6-YL)-(1-PHENYL-ETHYL)-AMINE
SpectraBase Compound ID LOj7j2ryFTy
InChI InChI=1S/C39H38NO4P/c1-29(30-19-9-4-10-20-30)40-45-43-38(31-21-11-5-12-22-31,32-23-13-6-14-24-32)35-36(42-37(2,3)41-35)39(44-45,33-25-15-7-16-26-33)34-27-17-8-18-28-34/h4-29,35-36,40H,1-3H3/t29-,35+,36+/m0/s1
InChIKey RPIFUXYBQXQITA-BXQIBZSOSA-N
Mol Weight 615.7 g/mol
Molecular Formula C39H38NO4P
Exact Mass 615.253846 g/mol
Enantiomer InChIKey RPIFUXYBQXQITA-QJFUKTLSSA-N

View Spectrum of (2,2-DIMETHYL-4,4,8,8-TETRAPHENYL-TETRAHYDRO-[1,3]-DIOXOLO-[4,5-E]-[1,3,2]-DIOXAPHOSPHEPIN-6-YL)-(1-PHENYL-ETHYL)-AMINE

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

View Spectrum of (2,2-DIMETHYL-4,4,8,8-TETRAPHENYL-TETRAHYDRO-[1,3]-DIOXOLO-[4,5-E]-[1,3,2]-DIOXAPHOSPHEPIN-6-YL)-(1-PHENYL-ETHYL)-AMINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
N-(MORPHOLINO)-TADDOL-PHOSPHORAMIDITE
N,N-METHYL,BENZYL-TADDOL-PHOSPHORAMIDITE
N,N-METHYL,PHENYL-TADDOL-PHOSPHORAMIDITE
(3aR,8aR)-2,2-dimethyl-4,4,6,8,8-pentakis-phenyl-3a,8a-dihydro-[1,3]dioxolo[4,5-e][1,3,2]dioxaphosphepin
9,9-Dimethyl-4-(4'-methylphenyl)-2,2,6,6-tetraphenyl-3,5,8,10-tetraoxa-4-phosphabicyclo[5.3.0]decane
(1R,7r,8R)-8,10,10-triphenyl-2,4,6,9-tetraoxabicyclo[5.3.0]decane
(4-R,5-R,1'-S,2'-S)-2-[2-[3-TERT.-BUTYL-(DIPHENYL)-SILOXYPROPYL]-CYCLOPROPYL]-4,5-BIS-[METHOXY-(DIPHENYL)-METHYL]-1,3,2-DIOXABOROLANE
1,4-Anhydro-1-(2,4-diamino-5-pyrimidinyl)-2,3-O-(1-methylethylidene)-5-O-tritylpentitol
2-{ Diphenyl [(trimethylsilyl)oxy] methyl }-2-ethoxy-4,4-diphenyl-4-[(trimethylsilyl)oxy] butane nitrile
(TRANS,TRANS)-N,N-PYRROLIDINYL-1-PHENYL-3-PYRROL-1-YLINDAN-2-CARBOXYAMIDE
Title Journal or Book Year
Copper-Catalyzed Asymmetric Conjugate Addition of Diethylzinc to α,β-Unsaturated Imines Derived from α-Aminoacids. Enantioselective Synthesis of γ-Substituted α-Dehydroaminoesters Organic Letters 2006
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