(2R)-2-([(TERT.-BUTYLOXY)-CARBONYL]-AMINO)-5-OXO-PHENYL-PENTANOIC-ACID,METHYLESTER
Compound with spectra: 1 NMR
![(2R)-2-([(TERT.-BUTYLOXY)-CARBONYL]-AMINO)-5-OXO-PHENYL-PENTANOIC-ACID,METHYLESTER](/api/compound/C6QKuyLfDwN.png?ph=true&h=300&w=458 "(2R)-2-([(TERT.-BUTYLOXY)-CARBONYL]-AMINO)-5-OXO-PHENYL-PENTANOIC-ACID,METHYLESTER")
| SpectraBase Compound ID | C6QKuyLfDwN |
|---|---|
| InChI | InChI=1S/C17H23NO5/c1-17(2,3)23-16(21)18-13(15(20)22-4)10-11-14(19)12-8-6-5-7-9-12/h5-9,13H,10-11H2,1-4H3,(H,18,21)/t13-/m1/s1 |
| InChIKey | WEYIBENIWMZWQA-CYBMUJFWSA-N |
| Mol Weight | 321.37 g/mol |
| Molecular Formula | C17H23NO5 |
| Exact Mass | 321.157623 g/mol |
| Enantiomer InChIKey | WEYIBENIWMZWQA-ZDUSSCGKSA-N |
| Racemate InChIKey | WEYIBENIWMZWQA-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
ALPHA-METHYL-GAMMA-BENZYL-(2R)-N-(TERT.-BUTOXYCARBONYL)-GLUTAMATE
Benzyl (2S)-2-tert-Butoxycarbonylamino-5-oxohexanoate
(S)-2-TERT.-BUTOXYCARBONYLAMINO-5-OXODECA-6-YNOIC-ACID-TERT.-BUTYLESTER
Boc-D-Glu-OBzl
TERT.-BUTYL-N-[(1R)-1-[(METHYLSULFONYLOXY)-METHYL]-4-OXO-4-PHENYLBUTYL]-CARBAMATE
(S,E)-4-ETHOXY-4-OXOBUT-2-ENYL_5-AMINO-2-(TERT.-BUTOXYCARBONYLAMINO)-5-OXOPENTANOATE
(2S)-2-(tert-butoxycarbonylamino)-6-keto-enanthic acid benzyl ester
(2R,5R)-2-(tert-butoxycarbonylamino)-5-hydroxy-6-trimethylsilyl-hexanoic acid ethyl ester
TERT.-BUTYL-6-AMINO-2-(TERT.-BUTOXYCARBONYLAMINO)-5,5-DIDEUTERIOHEXANOATE
DIBENZYL-CIS-2,9-BIS-(TERT.-BUTOXYCARBONYLAMINO)-DEC-5-ENEDIOATE
| Title | Journal or Book | Year |
|---|---|---|
| Approaches to the Synthesis of Cytochalasans Part9. A versatile concept leading to all structural types of cytochalasans | Helvetica Chimica Acta | 1990 |