(S)-2-TERT.-BUTOXYCARBONYLAMINO-4-OXO-6-PHENYLHEX-5-YNOIC-ACID-TERT.-BUTYLESTER
Compound with spectra: 1 NMR
| SpectraBase Compound ID | Ac5Iw2ojxa2 |
|---|---|
| InChI | InChI=1S/C21H27NO5/c1-20(2,3)26-18(24)17(22-19(25)27-21(4,5)6)14-16(23)13-12-15-10-8-7-9-11-15/h7-11,17H,14H2,1-6H3,(H,22,25)/t17-/m0/s1 |
| InChIKey | YTKNWZBSZINRQM-KRWDZBQOSA-N |
| Mol Weight | 373.45 g/mol |
| Molecular Formula | C21H27NO5 |
| Exact Mass | 373.188923 g/mol |
| Enantiomer InChIKey | YTKNWZBSZINRQM-QGZVFWFLSA-N |
| Racemate InChIKey | YTKNWZBSZINRQM-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
N-TERT.-BUTOXYCARBONYL-L-ASPARTIC-ACID-ALPHA-TERT.-BUTYLESTER-BETA-N-METHOXY-N-METHYLAMIDE
Benzyl 2(S)-[(tert-butoxycarbonyl)amino]-4-oxo-6-methylheptanoate
1-TERT.-BUTYL-5-METHYL-(2S)-N-TERT.-BUTOXYCARBONYL-4-METHYLENEGLUTAMATE
TERT.-BUTYL-(2S,4S)-N-TERT.-BUTOXYCARBONYL-5-TERT.-BUTYLDIMETHYLSILYLOXYLEUCINE
O,O-DIMETHANESULFONYL-(S)-N-BOC-5,5'-DIHYDROXYLEUCINE-TERT.-BUTYLESTER
N-TERT.-BUTOXYCARBONYL4-HYDROXYMETHYL-GLUTAMIC-ACID
1-TERT.-BUTYLHYDROGEN-(2S,4S)-N-TERT.-BUTOXYCARBONYL-4-ETHYLGLUTAMATE
TERT.-BUTYL-6-AMINO-2-(TERT.-BUTOXYCARBONYLAMINO)-4,4-DIDEUTERIOHEXANOATE
TERT.-BUTYL-2-(TERT.-BUTOXYCARBONYLAMINO)-5-CYANO-4,4-DIDEUTERIOPENTANOATE
Benzyl 2(S)-[(tert-Butoxycarbonyl)amino]-4(R/S)-(chloromethyl)hex-5-enoate
| Title | Journal or Book | Year |
|---|---|---|
| The synthesis of pyrimidin-4-yl substituted α-amino acids. A versatile approach from alkynyl ketones | Journal of the Chemical Society, Perkin Transactions 1 | 1999 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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