49;METHYL-(1RS,3ASR,4RS,7RS,7ASR)-4-[(1,3-DITHIAN-2-YL)-METHYL]-1,2,3,4,7,7A-HEXAHYDRO-6,7-DIMETHYL-3-OXO-1-(PHENYLMETHYL)-3AH-ISOINDOLE-3A-CARBOXYLATE
Compound with spectra: 1 NMR
![49;METHYL-(1RS,3ASR,4RS,7RS,7ASR)-4-[(1,3-DITHIAN-2-YL)-METHYL]-1,2,3,4,7,7A-HEXAHYDRO-6,7-DIMETHYL-3-OXO-1-(PHENYLMETHYL)-3AH-ISOINDOLE-3A-CARBOXYLATE](/api/compound/7LupqpSeqMM.png?ph=true&h=300&w=458 "49;METHYL-(1RS,3ASR,4RS,7RS,7ASR)-4-[(1,3-DITHIAN-2-YL)-METHYL]-1,2,3,4,7,7A-HEXAHYDRO-6,7-DIMETHYL-3-OXO-1-(PHENYLMETHYL)-3AH-ISOINDOLE-3A-CARBOXYLATE")
| SpectraBase Compound ID | 7LupqpSeqMM |
|---|---|
| InChI | InChI=1S/C24H31NO3S2/c1-15-12-18(14-20-29-10-7-11-30-20)24(23(27)28-3)21(16(15)2)19(25-22(24)26)13-17-8-5-4-6-9-17/h4-6,8-9,12,16,18-21H,7,10-11,13-14H2,1-3H3,(H,25,26)/t16-,18-,19+,21+,24-/m1/s1 |
| InChIKey | XVRHLRBCPNIMPO-GVLXJJNQSA-N |
| Mol Weight | 445.64 g/mol |
| Molecular Formula | C24H31NO3S2 |
| Exact Mass | 445.174536 g/mol |
| Enantiomer InChIKey | XVRHLRBCPNIMPO-LESZHHMGSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
Methyl 4-{2'-(t-butyl)dimethylsilyloxy]ethyl}-1,2,3,4,7,7a-hexahydro-6,7-dimethyl-3-oxo-1-(phenylmethyl)-3aH-isoindole-3a-carboxylate
METHYL-(1RS,3ASR,4RS,7RS,7ASR)-4-(FORMYLMETHYL)-1,2,3,4,7,7A-HEXAHYDRO-6,7-DIMETHYL-3-OXO-1-(PHENYLMETHYL)-3AH-ISOINDOLE-3A-CARBOXYLATE
1H,9H-Furo[3,4-d]isoindole-1,9-dione, 3,3a,6,6a,7,8-hexahydro-5,6-dimethyl-7-(phenylmethyl)-, (3a.alpha.,6.beta.,6a.beta.,7.alpha.,9aS*)-
Phenochalasin G
L-696,475
3-(3-bromo-5-ethoxy-4-hydroxyphenyl)-5-(4-methylphenyl)-2-phenyldihydro-2H-pyrrolo[3,4-d]isoxazole-4,6(3H,5H)-dione
ethyl 2-({[3-chloro-5-phenyl-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-2-yl]carbonyl}amino)-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylate
(13E,16S,17R,18R)-17,18-Epoxy-16,18-dimethyl-10-phenyl[11]cytochalasa-6(7),13-dien-1,21-dione
PHENOCHALASIN-A
| Title | Journal or Book | Year |
|---|---|---|
| Approaches to the Synthesis of Cytochalasans. Part 11. Further transformations and cyclization attempts directed towards proxiphomin | Helvetica Chimica Acta | 1993 |