(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 |
[2S,3R,4S,5S,(7E)]-2,4-DIACETOXY-N-BENZYL-5-(TERT.-BUTYLDIPHENYLSILYLOXY)-8-PHENYL-3-(TOSYLAMINO)-OCT-7-ENAMIDE
(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
(6'E)-1'-(Isocopal-12-en-15-yl)-8'-[(t-butyldiphenylsilyl)oxy]-3'-hydroxy-6'-methyloct-6'-ene-2'-carbonitrile
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
Methyl (2'E,6'Z)-1'-(Isocopal-12-en-15-yl)-8'-[(t-butyldiphenylsilyl)oxy]-6'-methylocta-2',6'-diene-2'-carboxylate
2-CHLORO-9-[2-DEOXY-5-O-[(1,1-DIMETHYLETHYL)-DIPHENYLSILYL]-3-O-(PHENOXYTHIOCARBONYL)-BETA-D-ERYTHRO-PENTOFURANOSYL]-9H-PURIN-6-AMINE
| 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 |