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(1R*,4R*,5R*,6S*)-N-PHENYL-8-TRIISOPROPYLSILYLOXY-2-THIABICYCLO-[2.2.2]-OCT-7-ENE-5,6-DICARBOXILIC-ACID-IMIDE

Compound with spectra: 1 NMR

(1R*,4R*,5R*,6S*)-N-PHENYL-8-TRIISOPROPYLSILYLOXY-2-THIABICYCLO-[2.2.2]-OCT-7-ENE-5,6-DICARBOXILIC-ACID-IMIDE
SpectraBase Compound ID A1FTUiMYh0B
InChI InChI=1S/C24H33NO3SSi/c1-14(2)30(15(3)4,16(5)6)28-19-12-20-22-21(18(19)13-29-20)23(26)25(24(22)27)17-10-8-7-9-11-17/h7-12,14-16,18,20-22H,13H2,1-6H3/t18-,20+,21+,22-/m0/s1
InChIKey HPAHROUQSKFZAG-PDGJWGCVSA-N
Mol Weight 443.7 g/mol
Molecular Formula C24H33NO3SSi
Exact Mass 443.195042 g/mol
Enantiomer InChIKey HPAHROUQSKFZAG-RYFAJOAYSA-N

View Spectrum of (1R*,4R*,5R*,6S*)-N-PHENYL-8-TRIISOPROPYLSILYLOXY-2-THIABICYCLO-[2.2.2]-OCT-7-ENE-5,6-DICARBOXILIC-ACID-IMIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(1R*,4R*,5R*,6S*)-N-PHENYL-8-TERT.-BUTYLDIMETHYLSILYLOXY-2-THIABICYCLO-[2.2.2]-OCT-7-ENE-5,6-DICARBOXILIC-ACID-IMIDE
(1S*,4S*,5R*,6S*)-N-PHENYL-7-TRIISOPROPYLSILYLOXY-2-THIABICYCLO-[2.2.2]-OCT-7-ENE-5,6-DICARBOXILIC-ACID-IMIDE
(1S*,4S*,5R*,6S*)-N-phenyl-7-triisopropylsilyloxy-2-thiabicyclo[2.2.2]oct-7-ene-5,6-dicarboxylic Acid Imide
(3aR*,4S*,7R*,7aS*)-3a,4,7,7a-Tetrahydro-9,9-dimethyl-2-phenyl-5-(trimethylsiloxy)-4,7-ethanoisoindole-1,3-dione
2-(3-(3,4-dichlorophenyl)-5,6-dimethyl-2,4-dioxo-3,4-dihydrothieno[2,3-d]pyrimidin-1(2H)-yl)-N-phenylacetamide
19-HYDROXY-ROYLEANONE
#33;2-(TERT.-BUTYLDIPHENYLSILYLOXY)-ETHYL-3-[[3-[4-(3-ACETAMIDOPHENYL)-PIPERIDIN-1-YL]-PROPYL]-CARBAMOYL]-4-(3,4-DIFLUOROPHENYL)-6-(METHOXYMETHYL)-2-OXO-1,2,3,
N'-[(E)-(3,5-ditert-butyl-4-hydroxyphenyl)methylidene]-2-{[3-(4-methylphenyl)-4-oxo-3,4,5,6,7,8-hexahydro[1]benzothieno[2,3-d]pyrimidin-2-yl]sulfanyl}acetohydrazide
(+-)-5,7-Dichloro-9-ethyl-8-methyl-2-phenyl-3a,4,9,9a-tetrahydro-1H-pyrrolo[3,4-g]isoquinoline-1,3(2H)-dione
3-(4-chlorophenyl)-5,6-dimethyl-1-[2-(2-methyl-1-piperidinyl)-2-oxoethyl]thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione
Title Journal or Book Year
Diels–Alder reactions of activated 2H-thiopyrans Canadian Journal of Chemistry 1991
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