TERT.-BUTYL-(3R,ALPHA-R)-(E)-3-[N-(ALPHA-METHYLBENZYL)-AMINO]-HEX-4-ENOATE
Compound with spectra: 1 NMR
![TERT.-BUTYL-(3R,ALPHA-R)-(E)-3-[N-(ALPHA-METHYLBENZYL)-AMINO]-HEX-4-ENOATE](/api/compound/4XqYNtWWCQL.png?ph=true&h=300&w=458 "TERT.-BUTYL-(3R,ALPHA-R)-(E)-3-[N-(ALPHA-METHYLBENZYL)-AMINO]-HEX-4-ENOATE")
| SpectraBase Compound ID | 4XqYNtWWCQL |
|---|---|
| InChI | InChI=1S/C18H27NO2/c1-6-10-16(13-17(20)21-18(3,4)5)19-14(2)15-11-8-7-9-12-15/h6-12,14,16,19H,13H2,1-5H3/b10-6+/t14-,16?/m1/s1 |
| InChIKey | VCKFKJYATIDRTA-IQSGDQAVSA-N |
| Mol Weight | 289.42 g/mol |
| Molecular Formula | C18H27NO2 |
| Exact Mass | 289.204179 g/mol |
| Enantiomer InChIKey | VCKFKJYATIDRTA-AYQDKZTOSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3S,.alpha.R)-Ethyl 3-[N-(.alpha.-methylbenzyl)amino]-4,4-dimethylpentanoate
2,2-dimethyl-N-(1-phenylethyl)tetrahydro-2H-pyran-4-amine
(R)tert-Butyl 3-[N-allyl-N-(1-phenylethyl)amino]propanoate
(E)-5-[[(1R)-1-phenylethyl]amino]-7-trimethylsilyl-hept-2-en-6-ynoic acid methyl ester
cis-2-Ethyl-N-(1-phenyl-ethyl)-cyclohexanamine
cis-(+)-(alpha-R,1R,2S)-N-(2-ethylcyclohexyl)-alpha-methylbenzylamine, hydrochloride
(S/R,S)-N-(1-Cyclohexylpentyl)-N-(1-phenylethyl)amine
CIS-2,6-DIPHENYL-CIS-4-HYDROXYPIPERIDINE
CIS-2,6-DIPHENYL-TRANS-4-HYDROXYPIPERIDINE
| 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 |