(3S,ALPHA-R)-(E)-3-[N-BENZYL-N-(ALPHA-METHYLBENZYL)-AMINO]-HEX-4-ENOIC-ACID
Compound with spectra: 1 NMR
![(3S,ALPHA-R)-(E)-3-[N-BENZYL-N-(ALPHA-METHYLBENZYL)-AMINO]-HEX-4-ENOIC-ACID](/api/compound/HXnpcm2YYWy.png?ph=true&h=300&w=458 "(3S,ALPHA-R)-(E)-3-[N-BENZYL-N-(ALPHA-METHYLBENZYL)-AMINO]-HEX-4-ENOIC-ACID")
| SpectraBase Compound ID | HXnpcm2YYWy |
|---|---|
| InChI | InChI=1S/C21H25NO2/c1-3-10-20(15-21(23)24)22(16-18-11-6-4-7-12-18)17(2)19-13-8-5-9-14-19/h3-14,17,20H,15-16H2,1-2H3,(H,23,24)/b10-3+/t17-,20-/m1/s1 |
| InChIKey | NHDANXWMDZDAKF-TWNLFCHXSA-N |
| Mol Weight | 323.44 g/mol |
| Molecular Formula | C21H25NO2 |
| Exact Mass | 323.188529 g/mol |
| Enantiomer InChIKey | NHDANXWMDZDAKF-XKHZYSMTSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
TERT.-BUTYL-(3S,ALPHA-R)-(E)-3-[N-ALLYL-N-(ALPHA-METHYLBENZYL)-AMINO]-HEX-4-ENOATE
1-Benzyl-2-methyl-6-phenyl-1,2,3,6-tetrahydropyridine
(2S,6R)-1-benzyl-2-methyl-6-phenyl-3,6-dihydro-2H-pyridine
(E)-(2S*,5R*)-2-Acetoxy-5-[benzyl(diphenylmethyl)amino]hex-3-ene
2-Acetoxy-5-[benzyl(diphenylmethyl)amino]-hex-2-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-phenylpropanoate
ISOPROPYL-3-DIBENZYLAMINO-3-(4-METHOXYPHENYL)-PROPANOATE
PQMOBQAUCBGSSD-UHFFFAOYSA-N
(+)-N-(1-Hydroxymethyl-2-phenylethyl)-N-(1-phenylethyl)acetamide
| 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 |