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TRICARBONYL-[(8,9,11,12,13,14-ETA)-13-METHOXY-TOTARA-8,11,13-TRIENE]-CHROMIUM;ALPHA-DIASTEREOMER

Compound with spectra: 4 NMR

TRICARBONYL-[(8,9,11,12,13,14-ETA)-13-METHOXY-TOTARA-8,11,13-TRIENE]-CHROMIUM;ALPHA-DIASTEREOMER
SpectraBase Compound ID a3go7GfL5M
InChI InChI=1S/C21H32O.3CO.Cr/c1-14(2)19-15-8-11-18-20(3,4)12-7-13-21(18,5)16(15)9-10-17(19)22-6;3*1-2;/h9-10,14,18H,7-8,11-13H2,1-6H3;;;;/t18?,21-;;;;/m1..../s1
InChIKey IQLHRKWDUZVCLP-HJJPMOALSA-N
Mol Weight 436.5 g/mol
Molecular Formula C24H32CrO4
Exact Mass 436.170565 g/mol
Enantiomer InChIKey IQLHRKWDUZVCLP-YKRWVJKJSA-N

View Spectrum of TRICARBONYL-[(8,9,11,12,13,14-ETA)-13-METHOXY-TOTARA-8,11,13-TRIENE]-CHROMIUM;ALPHA-DIASTEREOMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6

View Spectrum of TRICARBONYL-[(8,9,11,12,13,14-ETA)-13-METHOXY-TOTARA-8,11,13-TRIENE]-CHROMIUM;ALPHA-DIASTEREOMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CCl4

View Spectrum of TRICARBONYL-[(8,9,11,12,13,14-ETA)-13-METHOXY-TOTARA-8,11,13-TRIENE]-CHROMIUM;ALPHA-DIASTEREOMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6

View Spectrum of TRICARBONYL-[(8,9,11,12,13,14-ETA)-13-METHOXY-TOTARA-8,11,13-TRIENE]-CHROMIUM;ALPHA-DIASTEREOMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CCl4
  • TRICARBONYL-[(8,9,11,12,13,14-ETA)-13-METHOXY-TOTARA-8,11,13-TRIENE]-CHROMIUM;BETA-DIASTEREOMER
Chromium, tricarbonyl[(4b,5,6,7,8,8a-.eta.)-1,2,3,4,4a,9,10,10a-octahydro-7-methoxy-1,14a-trimethyl-8-(1-methylethyl)phenanthrene]-, stereoisomer
Laminat VII31-0164+HX+DMP 30
Tricarbonyl-{2-[.eta(6).-3',5'-dimethoxy-4'-(trimethylsilyl)phenyl]-(methyldiethyl)phosphonate]-chromium ( 0 )
Tricarbonyl-{2-[.eta(6).-3',5'-dimethoxy-4'-(trimethylsilyl)phenyl]-1-(4"-methoxyphenyl)ethene}-chromium ( 0 )
IRGANOX B 501 W
Poly(ethylene glycol), reacted with Bisphenol A diglycidyl ether
{ .eta(2).-P, P-[2,2-bis( Diphenylphosphanylmethyl)-2-(piperidinomethyl)propane ] tetracarbonyl molybdenium ( 0)
20-Deethyl-3-benzoyloxy-4-benzyl-2,16-didehydro-16-(methoxycarbonyl)-3,4-seco-20-epi-aspidospermidine
cis-2 : 3 ; 9 : 10-Dicyclohexane[5,7,12,14]tetramethyl[1,4,8,11]-N,N,N,N-tetraazacyclotetradecane nickel (II) acetate
Tricarbonyl-{2-[.eta(6).-3',5'-dimethoxy-4'-(trimethylsilyl)phenyl]-1-(4"-methoxyphenyl)ethanol}-chromium ( 0 )
D-3-METHOXY-17.ALPHA.-HYDROXY-9(11)-SECOESTRA-1,3,5(10),6,8-PENTAEN-11,17.BETA.-DIOIC ACID LACTONE (11-17) 17-METHYL ESTER
Title Journal or Book Year
Phenolic Oxidations of Totarol Australian Journal of Chemistry 1990
Other Resources
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