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(S)-2-[BIS-(TERT.-BUTYLOXYCARBONYL)-AMINO]-GLUTARSAEURE-5-BENZYL-1-(TERT.-BUTYL)-ESTER

Compound with spectra: 1 NMR, and 1 MS (GC)

(S)-2-[BIS-(TERT.-BUTYLOXYCARBONYL)-AMINO]-GLUTARSAEURE-5-BENZYL-1-(TERT.-BUTYL)-ESTER
SpectraBase Compound ID IfGltFl8UUX
InChI InChI=1S/C26H39NO8/c1-24(2,3)33-21(29)19(15-16-20(28)32-17-18-13-11-10-12-14-18)27(22(30)34-25(4,5)6)23(31)35-26(7,8)9/h10-14,19H,15-17H2,1-9H3/t19-/m0/s1
InChIKey WVTNKUKWZXIHGH-IBGZPJMESA-N
Mol Weight 493.6 g/mol
Molecular Formula C26H39NO8
Exact Mass 493.267567 g/mol
Enantiomer InChIKey WVTNKUKWZXIHGH-LJQANCHMSA-N
Racemate InChIKey WVTNKUKWZXIHGH-UHFFFAOYSA-N

View Spectrum of (S)-2-[BIS-(TERT.-BUTYLOXYCARBONYL)-AMINO]-GLUTARSAEURE-5-BENZYL-1-(TERT.-BUTYL)-ESTER

MS (GC) Spectrum
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Source of Spectrum H-73-408-13

View Spectrum of (S)-2-[BIS-(TERT.-BUTYLOXYCARBONYL)-AMINO]-GLUTARSAEURE-5-BENZYL-1-(TERT.-BUTYL)-ESTER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • L-Glutamic acid, N,N-bis[(1,1-dimethylethoxy)carbonyl]-, 1-(1,1-dimethylethyl) 5-(phenylmethyl) ester
(2S,4S)-2-DITERT.-BUTOXYCARBONYLAMINO-4-METHYLPENTANE-1,5-DIOIC-ACID-1-TERT.-BUTYLESTER
tert-Butyl N-(tert-butoxycarbonyl)-L-pyroglutamate
(2S,5R/S)-1-(tert-Butoxycarbonyl)-5-hydroxypyrrolidine-2-carboxylic acid tert-butyl ester
TERT.-BUTYL-(2S)-N-TERT.-BUTYLOXYCARBONYL-4-METHYLIDENE-PROLINATE
(4S)-3-Benzyloxycarbonyl-4-(4'acetyl-3'-oxobutyl)oxazolidin-5-one
(2S)-2-(tert-Butoxycarbonylmethoxymethylamino)-3-phenylpropionoic acid 5-[(2S)-2-(tert-butoxycarbonylmethoxymethylamino)-3-phenylpropionyloxy]pentyl ester
(2S)-2-(tert-Butoxycarbonylmethoxymethylamino)-3-phenylpropionoic acid 4-[(2S)-2-(tert-butoxycarbonylmethoxymethylamino)-3-phenylpropionyloxy]butyl ester
1-(tert-butyl) 2-methyl (2S,4S)-4-formylpyrrolidine-1,2-dicarboxylate
(2S,3S)-3-methyl-4-oxoazetidine-1,2-dicarboxylic acid O1-tert-butyl ester O2-methyl ester
(S)-1-(TERT.-BUTYLOXYCARBONYL)-5-(TRITYLOXYMETHYL)-2-PYRROLIDINONE
Title Journal or Book Year
Herstellung von ?Semialdehyd?-Derivaten von Asparagins�ure- und Glutamins�ure durchRosenmund-Reduktion Helvetica Chimica Acta 1990
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