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DIMETHYL-(R)-(+)-1-DIAZO-2-OXO-N-(TERT.-BUTOXYCARBONYL)-4-AMINO-5,5-DIMETHYL-HEXYLPHOSPHONATE

Compound with spectra: 2 NMR

DIMETHYL-(R)-(+)-1-DIAZO-2-OXO-N-(TERT.-BUTOXYCARBONYL)-4-AMINO-5,5-DIMETHYL-HEXYLPHOSPHONATE
SpectraBase Compound ID BihAv2qNF8b
InChI InChI=1S/C15H28N3O6P/c1-14(2,3)11(17-13(20)24-15(4,5)6)9-10(19)12(18-16)25(21,22-7)23-8/h11H,9H2,1-8H3,(H,17,20)/t11-/m1/s1
InChIKey LTZNWSLRVOQVMJ-LLVKDONJSA-N
Mol Weight 377.38 g/mol
Molecular Formula C15H28N3O6P
Exact Mass 377.171573 g/mol
Enantiomer InChIKey LTZNWSLRVOQVMJ-NSHDSACASA-N
Racemate InChIKey LTZNWSLRVOQVMJ-UHFFFAOYSA-N

View Spectrum of DIMETHYL-(R)-(+)-1-DIAZO-2-OXO-N-(TERT.-BUTOXYCARBONYL)-4-AMINO-5,5-DIMETHYL-HEXYLPHOSPHONATE

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

View Spectrum of DIMETHYL-(R)-(+)-1-DIAZO-2-OXO-N-(TERT.-BUTOXYCARBONYL)-4-AMINO-5,5-DIMETHYL-HEXYLPHOSPHONATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
DIMETHYL-(S)-(-)-1-DIAZO-2-OXO-N-(TERT.-BUTOXYCARBONYL)-4-AMINO-OCTYLPHOSPHONATE
(R)-Methyl 5-(tert-butoxycarbonylamino)-5-cyclohexyl-2-diazo-3-oxopentanoate
Diethyl (4R)-1-Diazo-4-hydroxy-4-(4-methoxyphenyl)-2-oxobutylphosphonate
Diethyl (4R)-1-Diazo-4-hydroxy-4-(4-methylphenyl)-2-oxobutylphosphonate
(3S,4S)-4-[[(1,1-dimethylethoxy)carbonyl]amino]-6-methyl-3-[[(phenylmethoxy)carbonyl]amino]heptanoic acid
(3R,4S)-4-[[(1,1-dimethylethoxy)carbonyl]amino]-6-methyl-3-[[(phenylmethoxy)carbonyl]amino]heptanoic acid
DIMETHYL-(R)-(-)-4-AMINO-3-OXO-1-PHENYLHEPTANYL-4-PHOSPHONATE
(3S,5S,1'S)-5-[1-(TERT.-BUTYLOXYCARBONYLAMINO)-3-METHYLBUTYL]-3-METHYLTETRAHYDROFURAN-2-ONE
(2S,3S,RS)-(tert-Butyl)-2-cyano-5-methyl-1-(p-tolylsulfinyl)hexan-3-ylcarbamate
butanoic acid, 4-[(2-amino-1-methyl-2-oxoethyl)amino]-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-oxo-, phenylmethyl ester
Title Journal or Book Year
Asymmetric Synthesis of Cis-5-Substituted Pyrrolidine 2-Phosphonates Using Metal Carbenoid NH Insertion and δ-Amino β-Ketophosphonates Organic Letters 2004
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