N-METHOXYCARBONYL-3-EXO-(3-PYRIDYL)-2-ENDO-(PARA-TOLYLSULFONYL)-7-AZABICYCLO-[2.2.1]-HEPTANE
Compound with spectra: 1 NMR
![N-METHOXYCARBONYL-3-EXO-(3-PYRIDYL)-2-ENDO-(PARA-TOLYLSULFONYL)-7-AZABICYCLO-[2.2.1]-HEPTANE](/api/compound/6iyM4Nvj3Wx.png?ph=true&h=300&w=458 "N-METHOXYCARBONYL-3-EXO-(3-PYRIDYL)-2-ENDO-(PARA-TOLYLSULFONYL)-7-AZABICYCLO-[2.2.1]-HEPTANE")
| SpectraBase Compound ID | 6iyM4Nvj3Wx |
|---|---|
| InChI | InChI=1S/C20H22N2O4S/c1-13-5-7-15(8-6-13)27(24,25)19-17-10-9-16(22(17)20(23)26-2)18(19)14-4-3-11-21-12-14/h3-8,11-12,16-19H,9-10H2,1-2H3/t16-,17+,18-,19-/m0/s1 |
| InChIKey | SWSAVUGSCNEMIR-RDGPPVDQSA-N |
| Mol Weight | 386.47 g/mol |
| Molecular Formula | C20H22N2O4S |
| Exact Mass | 386.130028 g/mol |
| Enantiomer InChIKey | SWSAVUGSCNEMIR-FCGDIQPGSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
N-METHOXYCARBONYL-3-EXO-(2-CHLORO-5-PYRIDYL)-2-ENDO-(PARA-TOLYLSULFONYL)-7-AZABICYCLO-[2.2.1]-HEPTANE
(S,S)-PH2P-N-2-NAPHTHOYL-DI-M-XYLYL-IMIDAZOLINE
5a,10b-dihydro-3,4,5a,7,8-pentamethylbenzofuro[2,3-b]benzofuran-10b-carboxylic acid, ethyl ester
Dimethyl 12,12'-dimethoxy-13,13'-bi(podocarpa-8,11,13-trien-19-oate
Methyl 2-[3-(4-Chlorophenyl)-4-oxo-1,9b-dihydro-4H-furo[3,4-c]-chromen-1-yl]acrylate
2,4(1H,3H)-Pyrimidinedione, 5-[2-O-[bis[(trimethylsilyl)oxy]phosphinyl]-3,5-bis-O-(trimethylsilyl)-.beta.-D-ribofuranosyl]-1,3-bis(trimethylsilyl)-
8,10-bis(chloranyl)-6a-(trifluoromethyl)-12H-[1,3]benzoxazino[3,2-a][3,1]benzoxazin-5-one
Benzoxepino[4,3,2-cd]isoindol-2(1H)-one, 11,11a-dihydro-5,7,8-trimethoxy-1-methyl-, (.+-.)-
2-(benzo[d][1,3]dioxol-6-yloxy)-3-(4-chlorophenyl)-5-mehylpyrimido[5,4-c]quinolin-4 (3H)-one
5-{1-[2-Amino-5-(4-methylphenyl)-1H-imidazol-4-yl]-2-(4-nitrophenyl)-2-oxoethyl}-6-hydroxy-1,3-dimethylpyrimidine-2,4(1H,3H)-dione
| Title | Journal or Book | Year |
|---|---|---|
| The total synthesis of the analgesic alkaloid epibatidine | Journal of the Chemical Society, Perkin Transactions 1 | 1998 |