2-[(1-PHENYLSULFONYL)-TRYPTOPHYL]-4-(TERT.-BUTOXYCARBONYL)-5-CYANO-6-METHOXY-7-(TRIMETHYLSILOXY)-1,2,5,6,7,8,9,10-OCTAHYDROISOQUINOLINE
Compound with spectra: 1 NMR
![2-[(1-PHENYLSULFONYL)-TRYPTOPHYL]-4-(TERT.-BUTOXYCARBONYL)-5-CYANO-6-METHOXY-7-(TRIMETHYLSILOXY)-1,2,5,6,7,8,9,10-OCTAHYDROISOQUINOLINE](/api/compound/68gZ1BR4kX9.png?ph=true&h=300&w=458 "2-[(1-PHENYLSULFONYL)-TRYPTOPHYL]-4-(TERT.-BUTOXYCARBONYL)-5-CYANO-6-METHOXY-7-(TRIMETHYLSILOXY)-1,2,5,6,7,8,9,10-OCTAHYDROISOQUINOLINE")
| SpectraBase Compound ID | 68gZ1BR4kX9 |
|---|---|
| InChI | InChI=1S/C35H45N3O6SSi/c1-35(2,3)43-34(39)29-23-37(21-25-19-31(44-46(5,6)7)33(42-4)28(20-36)32(25)29)18-17-24-22-38(30-16-12-11-15-27(24)30)45(40,41)26-13-9-8-10-14-26/h8-16,22-23,25,28,31-33H,17-19,21H2,1-7H3/t25-,28+,31-,32+,33-/m1/s1 |
| InChIKey | SSHHNDYIAAYAJQ-INRYUVOSSA-N |
| Mol Weight | 663.9 g/mol |
| Molecular Formula | C35H45N3O6SSi |
| Exact Mass | 663.279834 g/mol |
| Enantiomer InChIKey | SSHHNDYIAAYAJQ-GAOBKBBCSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
1H-Indole, 3-[[2-(1H-indol-3-yl)-4,6-dimethyl-3-cyclohexen-1-yl]carbonyl]-1-[(4-methylphenyl)sulfonyl]-, (1.alpha.,2.beta.,6.beta.)-(.+-.)-
(5-ETA-C5H5)-TICL2-[N-P-(TERT.-BUTYL)2-(2-CH2-PY)]
17.alpha.-(1,3-Dihydro-2H-inden-5-yl)-estradiol
Methyl 3,7-Diethyl-6-(4-methoxyphenyl)-2,3,6,7-tetrahydro-1H-azocino[5,4-b]indole-5-carboxylate
ethyl 4-(6-chloro-1,3-benzodioxol-5-yl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydro-3-quinolinecarboxylate
24(.xi.)-methylcholest-5-ene-1.alpha.,3.beta.,11.alpha.-triol
Diindolyl-methane compound of yohimbine (isomer 1)
Cholic acid, 4TMS
isobutyl 4-[2-(benzyloxy)phenyl]-7-(4-chlorophenyl)-2-methyl-5-oxo-1,4,5,6,7,8-hexahydro-3-quinolinecarboxylate
Cholic acid tetra(trimethylsilyl) ester
| Title | Journal or Book | Year |
|---|---|---|
| Formal total synthesis of deserpidine demonstrating a versatile amino-Claisen rearrangement/Wenkert cyclization strategy for the preparation of functionalized yohimbane ring systems | Journal of the American Chemical Society | 1990 |