(+/-)-[(5RS,6RS,9RS)-5,6,7,8,9,10-HEXAHYDRO-5,9-EPOXY-BENZOCYCLOOCTEN-6-YL]-4-METHYLBENZENESULFONATE
Compound with spectra: 1 NMR
![(+/-)-[(5RS,6RS,9RS)-5,6,7,8,9,10-HEXAHYDRO-5,9-EPOXY-BENZOCYCLOOCTEN-6-YL]-4-METHYLBENZENESULFONATE](/api/compound/DnJiDZxzDeh.png?ph=true&h=300&w=458 "(+/-)-[(5RS,6RS,9RS)-5,6,7,8,9,10-HEXAHYDRO-5,9-EPOXY-BENZOCYCLOOCTEN-6-YL]-4-METHYLBENZENESULFONATE")
| SpectraBase Compound ID | DnJiDZxzDeh |
|---|---|
| InChI | InChI=1S/C19H20O4S/c1-13-6-9-16(10-7-13)24(20,21)23-18-11-8-15-12-14-4-2-3-5-17(14)19(18)22-15/h2-7,9-10,15,18-19H,8,11-12H2,1H3/t15-,18-,19-/m0/s1 |
| InChIKey | ZDTCIOKTQIZIQS-SNRMKQJTSA-N |
| Mol Weight | 344.43 g/mol |
| Molecular Formula | C19H20O4S |
| Exact Mass | 344.10823 g/mol |
| Enantiomer InChIKey | ZDTCIOKTQIZIQS-ATZDWAIDSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
Ethyl (5RS,7RS,9RS)-(+-)-6-Oxo-5,6,7,8,9,10-hexahydro-5,9-epoxybenzocyclooctene-7-carboxylate
1,6-ANHYDRO-2-O-TOSYL-3,4-DI-O-TRIMETHYLSILYL-BETA-D-GLUCOPYRANOSE
METHYL-3-O-(4-O-BENZOYL-2,6-DIDEOXY-ALPHA-D-ARABINO-HEXOPYRANOSYL)-2,6-DIDEOXY-4-O-(PARA-TOLYLSULFONYL)-ALPHA-D-ARABINO-HEXOPYRANOSIDE
KFSYFZKIGKKAMO-AQNXPRMDSA-N
1,6-ANHYDRO-2-O-TOSYL-3-O-TRIMETHYLSILYL-4-O-METHYL-BETA-D-GLUCOPYRANOSE
(3R)-3-[(1R,3S)-4,6-dimethoxy-3-methyl-1,3-dihydroisobenzofuran-1-yl]-3-hydroxypropanoic acid methyl ester
2-o-Tosyl-4-(morpholinoamino)-4-deoxy-1,6-anhydro-.beta.-D-glucopyranose
2-O-TOZYL-4-N-AMINOMORPHOLYN-1,6-ANHYDRO-B-D-GLUCOPYRANOZIDE
1,3,3a,4,5,10,11,11a-octahydro-5,10-epoxy-4,11-ethanobenzo[5,6]cycloocta[1,2-c]furan
WTKADKWKAGFCHV-AQNXPRMDSA-N
| Title | Journal or Book | Year |
|---|---|---|
| Lipase-Catalyzed Kinetic Resolution of 2-Phenylethanol Derivatives and Chiral Oxa-Pictet-Spengler Reaction as the Key Steps in the Synthesis of Enantiomerically Pure Tricyclic Amines | European Journal of Organic Chemistry | 2012 |