(+/-)-(1-BETA,2-BETA,3-BETA)-1-(DIAZIDOMETHYL)-3-[(TRIISOPROPYLSILYL)-OXY]-CYCLOPENTAN-2-OL
Compound with spectra: 1 NMR
![(+/-)-(1-BETA,2-BETA,3-BETA)-1-(DIAZIDOMETHYL)-3-[(TRIISOPROPYLSILYL)-OXY]-CYCLOPENTAN-2-OL](/api/compound/LDPZDRmOkKc.png?ph=true&h=300&w=458 "(+/-)-(1-BETA,2-BETA,3-BETA)-1-(DIAZIDOMETHYL)-3-[(TRIISOPROPYLSILYL)-OXY]-CYCLOPENTAN-2-OL")
| SpectraBase Compound ID | LDPZDRmOkKc |
|---|---|
| InChI | InChI=1S/C15H30N6O2Si/c1-9(2)24(10(3)4,11(5)6)23-13-8-7-12(14(13)22)15(18-20-16)19-21-17/h9-15,22H,7-8H2,1-6H3/t12-,13-,14?/m1/s1 |
| InChIKey | NRSBKUCEYFCXNL-ZFXTZCCVSA-N |
| Mol Weight | 354.53 g/mol |
| Molecular Formula | C15H30N6O2Si |
| Exact Mass | 354.219951 g/mol |
| Enantiomer InChIKey | NRSBKUCEYFCXNL-RFHHWMCGSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(2S,5S,6S)-2-TRIISOPROPYLSILYLOXY-11,12-DIMETHYL-6-HYDROXY-8-PHENYL-7-OCTEN-4-ONE
(2S,5R,6R)-2-TRIISOPROPYLSILYLOXY-11,12-DIMETHYL-6-HYDROXY-8-PHENYL-7-OCTEN-4-ONE
(2S)-1-[(2S,4R,6S)-6-[2-[tert-butyl(dimethyl)silyl]oxyethyl]-4-tri(propan-2-yl)silyloxy-2-oxanyl]-4-penten-2-ol
1-[6-(2-tert-Butyldimethylsilyloxyethyl)-4-triisopropylsiloxytetrahydropyran-2-yl]pent-4-en-2-ol
(E)-(4R,5S,6R)-5,6-DI-(TERT.-BUTYLDIMETHYLSILOXY)-2,4-DIMETHYL-2-HEPTEN-1-OL
Methyl 12,13-bis(tert-butyldimethylsiloxy)octadec-9(z)-enoate
(3S,4S)-3,4-Bis(tert-butyldimethylsilyloxy)-7-phenylhept-1-en-6-yne
(E)-(4R,5S,6R)-5,6-DI-(TERT.-BUTYLDIMETHYLSILOXY)-2,4-DIMETHYL-2-HEPTENAL
(3S,5Z,10S,11R)-11,12-bis[(t-Butyldimethylsilyl)oxy]-3-[(2'-methoxyethoxy)methoxy]-10-methyldodec-5-en-2-one
Trimethylsilyl 2-[(1R,2R,3R)-2-[(Z)-pent-2-enyl]-3-trimethylsilyloxy-cyclopentyl]acetate
| Title | Journal or Book | Year |
|---|---|---|
| An allylic azide route to 4'-azido carbocyclic nucleosides. Synthesis of (.+-.)-(1'.alpha.,2'.alpha.,3'.beta.)- and (.+-.)-(1'.alpha.,2'.beta.,3'.beta.)-1-[1-azido-2-hydroxy-1-(hydroxymethyl)-3-cyclopentyl]thymine | The Journal of Organic Chemistry | 1992 |