(5S,6S)-6-[1-(TERT.-BUTYLDIPHENYLSILYLOXY)-BUT-3-ENYL]-3-(TRIFLUOROMETHYLSULFONYL)-FURAN-2(5H)-ONE
Compound with spectra: 1 NMR
![(5S,6S)-6-[1-(TERT.-BUTYLDIPHENYLSILYLOXY)-BUT-3-ENYL]-3-(TRIFLUOROMETHYLSULFONYL)-FURAN-2(5H)-ONE](/api/compound/7GQgYxKAK6E.png?ph=true&h=300&w=458 "(5S,6S)-6-[1-(TERT.-BUTYLDIPHENYLSILYLOXY)-BUT-3-ENYL]-3-(TRIFLUOROMETHYLSULFONYL)-FURAN-2(5H)-ONE")
| SpectraBase Compound ID | 7GQgYxKAK6E |
|---|---|
| InChI | InChI=1S/C25H27F3O6SSi/c1-5-12-20(21-17-22(23(29)32-21)33-35(30,31)25(26,27)28)34-36(24(2,3)4,18-13-8-6-9-14-18)19-15-10-7-11-16-19/h5-11,13-17,20-21H,1,12H2,2-4H3/t20-,21-/m0/s1 |
| InChIKey | BEQPOJPGAKRZBN-SFTDATJTSA-N |
| Mol Weight | 540.63 g/mol |
| Molecular Formula | C25H27F3O6SSi |
| Exact Mass | 540.124971 g/mol |
| Enantiomer InChIKey | BEQPOJPGAKRZBN-NHCUHLMSSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(7E)-5-O-TERT.-BUTYLDIPHENYLSILYL-8-PHENYL-6,7,8-TRIDEOXY-BETA-L-GULO-OCT-7-ENO-1,4-LACTONE
METHYL-4-O-BENZOYL-2-O-TERT.-BUTYLDIPHENYLSILYL-3,6-DIDEOXY-ALPHA-D-ARABINO-HEXOPYRANOSIDE
(6R,8R)-2,2,11,11-Tetramethyl-8-((2R,4R,5R)-4-methyl-5-(prop-2-yn-1-yl)tetrahydrofuran-2-yl)-3,3,10,10-tetraphenyl-4,9-dioxa-3,10-disiladodecan-6-ol
3,4-BIS-O-TERT.-BUTYL-DIPHENYLSILYL-6-O-FORMYL-D-GLUCAL
(4R,5R)-2,2-Dimethyl-4-(tert-Butyldimethylsiloxymethyl)-5-[1-(tert-butyldiphenylsilyloxy)butyl][1,3]dioxolane
(5R)-5-[tert-butyl(diphenyl)silyl]oxy-5-[(1S,2R)-2-[(E)-2-[(4R,5S)-2,2-dimethyl-5-[(Z)-oct-2-enyl]-1,3-dioxolan-4-yl]ethenyl]cyclopropyl]pentanoic acid methyl ester
1D-4,5-O-BISBENZOYL-1-O-(TERT.-BUTYLDIPHENYLSILYL)-MYO-INOSITOL
(6R,8R,11R,12R,E)-12-(2-(Benzyloxy)ethyl)-8-((tert-butyldiphenylsilyl)oxy)-14,14-diethyl-2,2,11-trimethyl-3,3-diphenyl-4,13-dioxa-3,14-disilahexadec-9-en-6-yl isobutyrate
1D-1-O-(TERT.-BUTYLDIPHENYLSILYL)-2,3,6-O-TRIS-(METHOXYMETHYLENE)-MYO-INOSITOL
(3AR,5R,6R,6AS)-6-ALLYL-5-[[TERT.-BUTYL-(DIPHENYL)-SILYL]-OXY]-1,3A,4,5,6,6A-HEXAHYDROPENTALEN-1-OL
| 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 |