(1R,4S,5S)-6-(BENZYLOXYCARBONYL)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE
Compound with spectra: 1 NMR
![(1R,4S,5S)-6-(BENZYLOXYCARBONYL)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE](/api/compound/J44cQYkBHOq.png?ph=true&h=300&w=458 "(1R,4S,5S)-6-(BENZYLOXYCARBONYL)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE")
| SpectraBase Compound ID | J44cQYkBHOq |
|---|---|
| InChI | InChI=1S/C29H31NO5Si/c1-29(2,3)36(22-15-9-5-10-16-22,23-17-11-6-12-18-23)34-20-24-25-26(27(31)35-24)30(25)28(32)33-19-21-13-7-4-8-14-21/h4-18,24-26H,19-20H2,1-3H3/t24-,25-,26-,30?/m1/s1 |
| InChIKey | YAGCIFKIYDCUPA-AKHSBFDASA-N |
| Mol Weight | 501.65 g/mol |
| Molecular Formula | C29H31NO5Si |
| Exact Mass | 501.19715 g/mol |
| Enantiomer InChIKey | YAGCIFKIYDCUPA-UENRUGSUSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(1R,4S,5S)-6-(TERT.BUTOXYCARBONYL)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE
N(DELTA)-(5-TERT.-BUTYLDIPHENYLSILYL-ALPHA-D-RIBOFURANOSYL)-N(ALPHA)-BENZYLOXYCARBONYL-ASPARAGINE-BENZYLESTER
(3S,4R,5S)-3-ACETOXY-5-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-4-(TOSYLAMINO)-TETRAHYDROFURAN-2-ONE
3-O-BENZYL-5-O-TERT.-BUTYL-DIPHENYLSILYL-1,2-O-ISOPROPYLIDENE-ALPHA-D-XYLOFURANOSE
METHYL-3-O-BENZYL-6-O-TERT.-BUTYLDIPHENYLSILYL-2-DEOXY-4-O-METHYLSULFONYL-BETA-D-LYXO-HEXOSIDE
METHYL-3-O-BENZYL-6-O-TERT.-BUTYLDIPHENYLSILYL-2-DEOXY-4-O-METHYLSULFONYL-ALPHA-D-XYLO-HEXOSIDE
1-{2-DEOXY-5-O-[(1,1-DIMETHYLETHYL)-DIPHENYLSILYL]-BETA-D-ERYTHRO-PENTOFURANOSYL}-1H-PYRROLO-[2,3-B]-PYRIDINE
(4R,5S)-3-N-tert-Butoxycarbonyl-4-tert-butyldiphenylsilyloxymethyl-5-hydroxymethyl-2,2-dimethyl-1,3-oxazolidine
5'-O-[(TERT.-BUTYL)-DIPHENYLSILYL]-1',2'-O-ISOPROPYLIDENE-BETA-D-ARABINOFURANOSIDE-3'H-PHOSPHONATE-TRIETHYLAMMONIUM-SALT
2'-MERCAPTOETHYL-4-AZIDO-3-O-BENZYL-6-O-TERT.-BUTYLDIPHENYLSILYL-1,2,4-TRIDEOXY-1-THIO-BETA-D-ARABINOSE-HEXOSIDE
| 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 |