(1R,4S,5S)-6-(TERT.BUTOXYCARBONYL)-4-[(1S)-1-(TERT.-BUTYLDIPHENYLSILYLOXY)-BUT-3-ENYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE
Compound with spectra: 1 NMR
![(1R,4S,5S)-6-(TERT.BUTOXYCARBONYL)-4-[(1S)-1-(TERT.-BUTYLDIPHENYLSILYLOXY)-BUT-3-ENYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE](/api/compound/25kBVN5GWui.png?ph=true&h=300&w=458 "(1R,4S,5S)-6-(TERT.BUTOXYCARBONYL)-4-[(1S)-1-(TERT.-BUTYLDIPHENYLSILYLOXY)-BUT-3-ENYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE")
| SpectraBase Compound ID | 25kBVN5GWui |
|---|---|
| InChI | InChI=1S/C29H37NO5Si/c1-8-15-22(25-23-24(26(31)33-25)30(23)27(32)34-28(2,3)4)35-36(29(5,6)7,20-16-11-9-12-17-20)21-18-13-10-14-19-21/h8-14,16-19,22-25H,1,15H2,2-7H3/t22-,23-,24+,25+,30?/m0/s1 |
| InChIKey | XRFHRJMDVLKZQM-ZJKPLRQGSA-N |
| Mol Weight | 507.7 g/mol |
| Molecular Formula | C29H37NO5Si |
| Exact Mass | 507.2441 g/mol |
| Enantiomer InChIKey | XRFHRJMDVLKZQM-GKJJZIIKSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
2.alpha.-Ethyl-1.alpha.-t-butyldiphenylsilyloxy-25-hydroxy-19-norvitamin D3
2.beta.-Ethyl-1.alpha.-t-butyldiphenylsilyloxy-25-dihydroxy-19-norvitamin D3
2.alpha.-Ethyl-3-t-butyldiphenylsilyloxy-1.alpha.,25-dihydroxy-19-norvitamin D3
1-[(2R,4S,5R)-5-[BIS-(4-METHOXYPHENYL)-PHENYLMETHOXYMETHYL]-4-(TERT.-BUTYLDIPHENYLSILANYLOXY)-TETRAHYDROFURAN-2-YL]-5-METHYL-1H-PYRIMIDINE-2,4-DIONE
N-ACETYL-(4S,5R,6S)-5-O-ACETYL-6-METHOXY-4-(1',2',3'-TRI-O-ACETYL-D-ERYTHRO-TRIITOL-1-YL)-TETRAHYDRO-1,3-OXAZINE-2-THIONE
N-ACETYL-(4S,5R,6R)-5-O-ACETYL-6-METHOXY-4-(1',2',3'-TRI-O-ACETYL-D-ERYTHRO-TRIITOL-1-YL)-TETRAHYDRO-1,3-OXAZINE-2-THIONE
BENZYL-BENZYL-[(S)-1-[(4S,5S)-2,2-DIMETHYL-5-[(R)-8,8,9,9-TETRAMETHYL-2,4,7-TRIOXA-8-SILADECAN-5-YL]-1,3-DIOXOLAN-4-YL]-BUT-3-ENYL]-CARBAMATE
(+/-)-2-EXO-(TERT.-BUTYL-DIPHENYL-SILANYLOXY)-9-EXO-HYDROXYMETHYL-4,8-DIOXA-TRICYCLO-[4.2.1.0(3,7)]-NONAN-5-OL
YSGQZEZSXQZIGD-ZEWOKLPPSA-N
N-(Benzyloxycarbonyl)-2-(2',3'-di-O-acetyl-5'-O-(t-butyl)diphenylsilyl]-.beta.-D-ribofuranosyl)-D,L-glycinenitrile
| 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 |