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0-[(1S)-5-EXO-CHLORO-1,5-ENDO-DIMETHYL-BICYCLO-[2.2.1]-HEPTANE-2-ENDO-CARBONYL]-D-PANTOLACTONE

Compound with spectra: 1 NMR

0-[(1S)-5-EXO-CHLORO-1,5-ENDO-DIMETHYL-BICYCLO-[2.2.1]-HEPTANE-2-ENDO-CARBONYL]-D-PANTOLACTONE
SpectraBase Compound ID 2lzuZabsYDb
InChI InChI=1S/C16H23ClO4/c1-14(2)8-20-13(19)11(14)21-12(18)10-5-9-6-15(10,3)7-16(9,4)17/h9-11H,5-8H2,1-4H3/t9-,10-,11-,15+,16-/m1/s1
InChIKey YYNNODITIGKKGV-STLRTNHMSA-N
Mol Weight 314.81 g/mol
Molecular Formula C16H23ClO4
Exact Mass 314.128487 g/mol
Enantiomer InChIKey YYNNODITIGKKGV-CKJIYCFSSA-N

View Spectrum of 0-[(1S)-5-EXO-CHLORO-1,5-ENDO-DIMETHYL-BICYCLO-[2.2.1]-HEPTANE-2-ENDO-CARBONYL]-D-PANTOLACTONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
O-((1S)-5-exo-Chloro-1,5-endo-dimethylbicyclo[2.2.1]hept-5-en-2-endo-carbonyl)-D-pantolactone
7-Desmethylasteriscanolide
7-Desmethylasteriscanolide-9H-epimer
(-)-METHYL-(1R,2R,4S,5S,6S,8S)-5-HYDROXY-8-ISOPROPYL-2,6-DIMETHYLBICYCLO-[2.2.2]-OCTANE-2-CARBOXYLATE
Dihydro-bakkenolide-A
Dihydro derivative of bakkenolides
(2R,3R,5S)-2-[(1S,2R)-1-hydroxy-6-keto-2-methyl-heptyl]-5-[(2R)-5-keto-2-methyl-tetrahydrofuran-2-yl]tetrahydrofuran-3-carboxylic acid
METHYL-6-CHLORO-UNDECACYCLO-[9.9.0.0(2,9).0(3,7).0(4,20).0(5,18).0(6,16).0(8,15).0(10,14).0(12,19).0(13,17)]-ICOSANECARBOXYLATE
(1S,8aS)-3-Acetoxyglycerol 2,5,5,8a-Tetramethyl-1,4,5,6,7,8-hexahydronaphthalene-1-carboxylate
Methyl 6-methyl-3-oxotricyclo[2.2.1.0(2,6)]heptane-1-carboxylate
Title Journal or Book Year
Stereoselection in thermal asymmetric Diels-Alder reactions. Electronic vs. steric effects The Journal of Organic Chemistry 1992
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