TERT.-BUTYL-(3S,ALPHA-R)-(E)-3-[N-ALLYL-N-(ALPHA-METHYLBENZYL)-AMINO]-HEX-4-ENOATE
Compound with spectra: 1 NMR
![TERT.-BUTYL-(3S,ALPHA-R)-(E)-3-[N-ALLYL-N-(ALPHA-METHYLBENZYL)-AMINO]-HEX-4-ENOATE](/api/compound/IrjRdwroNSX.png?ph=true&h=300&w=458 "TERT.-BUTYL-(3S,ALPHA-R)-(E)-3-[N-ALLYL-N-(ALPHA-METHYLBENZYL)-AMINO]-HEX-4-ENOATE")
| SpectraBase Compound ID | IrjRdwroNSX |
|---|---|
| InChI | InChI=1S/C21H31NO2/c1-7-12-19(16-20(23)24-21(4,5)6)22(15-8-2)17(3)18-13-10-9-11-14-18/h7-14,17,19H,2,15-16H2,1,3-6H3/b12-7+/t17-,19+/m1/s1 |
| InChIKey | YLVLWYOEAAYRHV-ZWSFKOMGSA-N |
| Mol Weight | 329.48 g/mol |
| Molecular Formula | C21H31NO2 |
| Exact Mass | 329.235479 g/mol |
| Enantiomer InChIKey | YLVLWYOEAAYRHV-HREHNZSSSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3S,ALPHA-R)-(E)-3-[N-BENZYL-N-(ALPHA-METHYLBENZYL)-AMINO]-HEX-4-ENOIC-ACID
(-)-(1R,1'S)-2-[1'-(4''-BROMOPHENYL)-ETHYL]-2-AZABICYCLO-[2.2.1]-HEPT-5-ENE
(3R)-N-Benzyl-1-{tert-butyl(dimethyl)silyl]oxy}-N-[(1R)-1-phenylethyl]-3-octanamine
(E),(S)-1-((S)-1-phenylhept-2-ynyl)pyrrolidine-2-carbaldehyde oxime
(E)-(2S*,5R*)-2-Acetoxy-5-[benzyl(diphenylmethyl)amino]hex-3-ene
(S)-3-(N-Benzyl-N-((R)-cyclohex-2-en-1-yl)amino)-N',N'-dimethylbutanamide
Ethyl 3-[N-Benzyl-N-(3-hydroxypropyl)amino]-3-(4-chlorophenyl)propanoate
1-Benzyl-2-methyl-6-phenyl-1,2,3,6-tetrahydropyridine
(2S,6R)-1-benzyl-2-methyl-6-phenyl-3,6-dihydro-2H-pyridine
N-[(S)-1'-Phenylethyl]-6-prop-2"-enyl-2-piperidone
| Title | Journal or Book | Year |
|---|---|---|
| Syntheses of derivatives of L-daunosamine and its C-3 epimer employing as the key step the asymmetric conjugate addition of a homochiral lithium amide to tert-butyl (E,E )-hexa-2,4-dienoate | Journal of the Chemical Society, Perkin Transactions 1 | 1999 |