(3S,4R,5S)-3-ACETOXY-4-[(ACETYL)-(TOSYL)-AMINO]-5-[(1S)-1-(TERT.-BUTYLDIPHENYLSILYLOXY)-BUT-3-ENYL]-TETRAHYDROFURAN-2-ONE
Compound with spectra: 1 NMR
![(3S,4R,5S)-3-ACETOXY-4-[(ACETYL)-(TOSYL)-AMINO]-5-[(1S)-1-(TERT.-BUTYLDIPHENYLSILYLOXY)-BUT-3-ENYL]-TETRAHYDROFURAN-2-ONE](/api/compound/9CNuk18R7pS.png?ph=true&h=300&w=458 "(3S,4R,5S)-3-ACETOXY-4-[(ACETYL)-(TOSYL)-AMINO]-5-[(1S)-1-(TERT.-BUTYLDIPHENYLSILYLOXY)-BUT-3-ENYL]-TETRAHYDROFURAN-2-ONE")
| SpectraBase Compound ID | 9CNuk18R7pS |
|---|---|
| InChI | InChI=1S/C35H41NO8SSi/c1-8-15-30(44-46(35(5,6)7,28-16-11-9-12-17-28)29-18-13-10-14-19-29)32-31(33(34(39)43-32)42-26(4)38)36(25(3)37)45(40,41)27-22-20-24(2)21-23-27/h8-14,16-23,30-33H,1,15H2,2-7H3/t30-,31+,32+,33-/m0/s1 |
| InChIKey | KREUNDREPHWSHT-FWGCVNADSA-N |
| Mol Weight | 663.9 g/mol |
| Molecular Formula | C35H41NO8SSi |
| Exact Mass | 663.232215 g/mol |
| Enantiomer InChIKey | KREUNDREPHWSHT-JDIHBLRXSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
N-(3-benzoyl-1,1-dioxido-2-pentyl-2H-1,2-benzothiazin-4-yl)-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)acetamide
METHYL_(PENTAFLUOROBENZYL_5-ACETAMIDO-4,7,8-TRI-O-ACETYL-9-(4-CHLOROBENZAMIDO)-3,5,9-TRIDEOXY-D-GLYCERO-ALPHA-D-GALACTO-2-NONULOPYRANOSID)-ONATE
METHYL_((2,3-DIFLUOROBENZYL)-5-CHLOROACETAMIDO-4,7,8-TRI-O-ACETYL-9-(4-CHLOROBENZAMIDO-3,5,9-TRIDEOXY-D-GLYCERO-ALPHA-D-GALACTO-2-NONULO
24(.xi.)-methylcholest-5-ene-1.alpha.,3.beta.,11.alpha.-triol
9H-Purine, 6-(5-methyl-2-furanyl)-9-(2,3,5-tri-O-acetyl-.beta.-D-ribofuranosyl)-
11H-4-thia-5,10,11c-triazacyclopenta[def]chrysen-11-one
Triethyl 5-tert-Butylimino-2-phenyldihydrofuran-2,3,4-tricarboxylate
Bronzaphyrin NS
WRRKUDUWTZOQNF-QRJAZEOMSA-N
METHYL_((2,3-DIFLUOROBENZYL)_5-FLUOROACETAMIDO-4,7,8-TRI-O-ACETYL-9-(4-CHLOROBENZAMIDO)-3,5,9-TRIDEOXY-D-GLYCERO-ALPHA-D-GALACTO-2-NONULO
| 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 |