(3S,4R,5S)-3-ACETOXY-4-[(ACETYL)-(TOSYL)-AMINO]-5-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-TETRAHYDROFURAN-2-ONE
Compound with spectra: 1 NMR
![(3S,4R,5S)-3-ACETOXY-4-[(ACETYL)-(TOSYL)-AMINO]-5-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-TETRAHYDROFURAN-2-ONE](/api/compound/2NhG1mf2JfF.png?ph=true&h=300&w=458 "(3S,4R,5S)-3-ACETOXY-4-[(ACETYL)-(TOSYL)-AMINO]-5-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-TETRAHYDROFURAN-2-ONE")
| SpectraBase Compound ID | 2NhG1mf2JfF |
|---|---|
| InChI | InChI=1S/C32H37NO8SSi/c1-22-17-19-25(20-18-22)42(37,38)33(23(2)34)29-28(41-31(36)30(29)40-24(3)35)21-39-43(32(4,5)6,26-13-9-7-10-14-26)27-15-11-8-12-16-27/h7-20,28-30H,21H2,1-6H3/t28-,29-,30+/m1/s1 |
| InChIKey | IRZAYWKNEZLLQS-OCBJUFRSSA-N |
| Mol Weight | 623.8 g/mol |
| Molecular Formula | C32H37NO8SSi |
| Exact Mass | 623.200915 g/mol |
| Enantiomer InChIKey | IRZAYWKNEZLLQS-OIFRRMEBSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3S,4R,5S)-3-ACETOXY-5-[[1S,(3E)]-1-(TERT.-BUTYLDIPHENYLSILYLOXY)-4-PHENYL-BUT-3-ENYL]-4-(TOSYLAMINO)-TETRAHYDROFURAN-2-ONE
5'-O-(TERT.-BUTYLDIPHENYLSILYL)-3'-O-[(2R,4S,5R)-3,4-DIMETHYL-5-PHENYL-1,3,2-OXAZAPHOSPHOLIDIN-2-YL]-THYMIDINE
9-[3-Azido-3-deoxy-5-O-(tert-butyldiphenylsilyl)-.beta.-D-xylofuranosyl]adenine
4-Methyl-10-methylene-1-p-toluenesulfonyl-3,6-dioxa-1-azaspiro[4.5]dec-7-en-2-one
REL-(3AR,5AR,6R,6AS,6BS)-METHYL-2-OXO-3-TOSYL-3,3A,5A,6,6A,6B-HEXAHYDRO-2H-CYCLOPROPA-[3,4]-BENZO-[1,2-D]-[1,3]-OXAZOLE-6-CARBOXYLATE
6-(4-{2-[3,5-bis-(tert-butyl-diphenyl-silanyloxy)-2-methylene-cyclohexylidene]-ethylidene}-7a-methyl-octahydro-inden-1-yl)-1,1-diphenyl-heptan-1-ol
2-CHLORO-9-[2-DEOXY-5-O-[(1,1-DIMETHYLETHYL)-DIPHENYLSILYL]-3-O-(PHENOXYTHIOCARBONYL)-BETA-D-ERYTHRO-PENTOFURANOSYL]-9H-PURIN-6-AMINE
3-(3-methylphenyl)-2-[(Z)-(2-oxo-1,2-dihydro-3H-indol-3-ylidene)methyl]-4(3H)-quinazolinone
(3aS,3bS,4aR,7S,7aS,8aR)-7-Bromo-2-methyl-octahydro-8-oxa-2,7b-diaza-dicyclopenta[a,e]pentalene-1,3-dione
1H-1,2,3-triazole-4,5-dicarboxylic acid, 1-[1-(phenylmethyl)-1H-benzimidazol-2-yl]-, dimethyl ester
| Title | Journal or Book | Year |
|---|---|---|
| Enantiospecific Synthesis of a Protected Equivalent of APTO, the β-Amino Acid Fragment of Microsclerodermins C and D, by Aziridino-γ-lactone Methodology | European Journal of Organic Chemistry | 2009 |