For citations & permissions, please see: Citations & Permissions - Wiley Science Solutions*

*Links on SpectraBase are not permalinks.

(E)-TERT.-BUTYL-(2S,4R)-4-[(E)-2-(METHYLPHENYLSULFONYL)-1-ETHENYL]-2-[(E)-(2-PHENYL-1-ETHENYL)-SULFANYLMETHYL]-PYRROLIDINE-1-CARBOXYLATE;MAJOR-I

Compound with spectra: 1 NMR

(E)-TERT.-BUTYL-(2S,4R)-4-[(E)-2-(METHYLPHENYLSULFONYL)-1-ETHENYL]-2-[(E)-(2-PHENYL-1-ETHENYL)-SULFANYLMETHYL]-PYRROLIDINE-1-CARBOXYLATE;MAJOR-I
SpectraBase Compound ID LrhCkS2T6jE
InChI InChI=1S/C27H33NO4S2/c1-21-10-12-25(13-11-21)34(30,31)17-15-23-18-24(28(19-23)26(29)32-27(2,3)4)20-33-16-14-22-8-6-5-7-9-22/h5-17,23-24H,18-20H2,1-4H3/b16-14+,17-15+/t23-,24-/m0/s1
InChIKey WVIAKRBJCRNPTC-KFSFDRMDSA-N
Mol Weight 499.7 g/mol
Molecular Formula C27H33NO4S2
Exact Mass 499.185101 g/mol
Enantiomer InChIKey WVIAKRBJCRNPTC-HZBJFGDESA-N

View Spectrum of (E)-TERT.-BUTYL-(2S,4R)-4-[(E)-2-(METHYLPHENYLSULFONYL)-1-ETHENYL]-2-[(E)-(2-PHENYL-1-ETHENYL)-SULFANYLMETHYL]-PYRROLIDINE-1-CARBOXYLATE;MAJOR-I

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(Z)-TERT.-BUTYL-(2S,4R)-4-[(E)-2-(METHYLPHENYLSULFONYL)-1-ETHENYL]-2-[(Z)-(2-PHENYL-1-ETHENYL)-SULFANYLMETHYL]-PYRROLIDINE-1-CARBOXYLATE;MINOR-I
TERT.-BUTYL-(2S,4R)-4-[(E)-2-METHYLOXYCARBONYL-1-ETHENYL]-2-[(E)-2-PHENYL-1-ETHENYLSULFINYLMETHYL]-PYRROLIDINE-1-CARBOXYLATE;MIXTURE
(1S,3R,4R)-3-Benzylsulfanylmethyl-2-azabicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester
1-tert-butyl 2-[2-(4-chlorophenyl)-2-oxoethyl] 4-hydroxy-1,2-pyrrolidinedicarboxylate
2,6-Ditert-butyl-4-[(Z)-1-phenyl-2-(p-tolylsulfonyl)vinyl]phenol
(3R,5S)-1-(TERT.-BUTYLOXYCARBONYL)-3-HYDROXY-5-(TRITYLOXYMETHYL)-2-PYRROLIDINONE
(1R,3S,4S)-N-Boc-2-azabicyclo[2.2.1]heptane-3-carboxylic acid
(3R)-N-Boc-2-azabicyclo[2.2.1]heptane-3-carboxylic acid
(1E,3E)-1-(Benzenesulfonyl)-2-butyl-4-phenyl-3-(tributylstannyl)-buta-1,3-diene
(2S,4S)-TERT.-BUTYL-N-TERT.-BUTOXYCARBNONYL-4-TRIFLUOROMETHYLPROLINATE
Title Journal or Book Year
Efficient Stereoselective Alkenylation through a Homolytic Domino Reaction Involving a 1,5 Sulfur-to-Carbon Translocation Journal of the American Chemical Society 2004
Other Resources
Unknown Identification

Search your unknown spectrum against the world's largest collection of reference spectra

KnowItAll Campus Solutions

KnowItAll offers faculty and students at your school access to all the tools you need for spectral analysis and structure drawing & publishing! Plus, access the world's largest spectral library.