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(1R,2S,3R,4S)-2-EXO-CYANO-3-EXO-PHENYLBICYCLO-[2.2.1]-HEPT-5-ENE-2-ENDO-CARBOXYLATE-OF-(S)-ETHYL-LACTATE

Compound with spectra: 2 NMR

(1R,2S,3R,4S)-2-EXO-CYANO-3-EXO-PHENYLBICYCLO-[2.2.1]-HEPT-5-ENE-2-ENDO-CARBOXYLATE-OF-(S)-ETHYL-LACTATE
SpectraBase Compound ID GT5J4erfdDE
InChI InChI=1S/C20H21NO4/c1-3-24-18(22)13(2)25-19(23)20(12-21)16-10-9-15(11-16)17(20)14-7-5-4-6-8-14/h4-10,13,15-17H,3,11H2,1-2H3/t13?,15-,16+,17+,20+/m1/s1
InChIKey XJCVKKOYLVYOQI-BQFHOOILSA-N
Mol Weight 339.39 g/mol
Molecular Formula C20H21NO4
Exact Mass 339.147058 g/mol
Enantiomer InChIKey XJCVKKOYLVYOQI-JSHIKVBVSA-N

View Spectrum of (1R,2S,3R,4S)-2-EXO-CYANO-3-EXO-PHENYLBICYCLO-[2.2.1]-HEPT-5-ENE-2-ENDO-CARBOXYLATE-OF-(S)-ETHYL-LACTATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (1R,2S,3R,4S)-2-EXO-CYANO-3-EXO-PHENYLBICYCLO-[2.2.1]-HEPT-5-ENE-2-ENDO-CARBOXYLATE-OF-(S)-ETHYL-LACTATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (1S,2R,3S,4R)-2-EXO-CYANO-3-EXO-PHENYLBICYCLO-[2.2.1]-HEPT-5-ENE-2-ENDO-CARBOXYLATE-OF-(S)-ETHYL-LACTATE
2-Cyano-3-phenyl-5-norbornene-2-carboxylic acid
(1S,2S,3R,4R)-2-ENDO-CYANO-3-ENDO-PHENYLBICYCLO-[2.2.1]-HEPT-5-ENE-2-EXO-CARBOXYLATE-OF-(S)-ETHYL-LACTATE
(1R,2R,3S,4S)-2-ENDO-CYANO-3-ENDO-PHENYLBICYCLO-[2.2.1]-HEPT-5-ENE-2-EXO-CARBOXYLATE-OF-(S)-ETHYL-LACTATE
3-Benzoyl-5,5-dicyano-1,3,5-triphenylcyclohex-1-ene
5(R)-[2(S)-Isoprpopyl-5(R)-methyl-(R)-cyclohexyloxy]-2(S)methyl-4-oxa-endo-tricyclo[5.2.1.0(2,6)]dec-8-en-3-one
Ethanone, 1-(octahydro-8-hydroxy-3,6,7,7-tetramethyl-3a,6-ethano-3aH-inden-5-yl)-, [3R-(3.alpha.,3a.beta.,5.beta.,6.beta.,7a.alpha.,8S*)]-
REL-[[(3AS,6S,6AR)-6A-METHYL-(1R,2S)-2-(2-PHENYLCYCLOHEXYL)-OXY]-3,3A,4,5,6-PENTAHYDROCYCLOPENTA-[D]-PYRROL-6-YL-N-OXIDE]-(2S)-HYDROXY-ACETIC-ACI
1-Methyl-estra-1,3,5(10),6-tetraen-17b-yl acetate
Rel-(6aS,10aS)-ethyl 9-methyl-6-oxo-6a,7,10,10a-tetrahydro-6H-benzo[c]chromene-6a-carboxylate
3-Oxo-guaia-10,14-epoxy-dilactone
Title Journal or Book Year
Asymmetric Diels-Alder reactions of chiral (E)-2-cyanocinnamates with cyclopentadiene The Journal of Organic Chemistry 1992
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