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#61B;MAJOR+MINOR;[(3-[(1S,4S,5R)-4-[4-(HYDROXYMETHYL)-PHENYL]-3-(TRIFLUOROMETHYLSULFONYL)-3-AZABICYCLO-[3.1.0]-HEXAN-1-YL]-5,6-DIHYDROPYRIDIN-1(2H)-(ISOXAZOL-5

Compound with spectra: 1 NMR

#61B;MAJOR+MINOR;[(3-[(1S,4S,5R)-4-[4-(HYDROXYMETHYL)-PHENYL]-3-(TRIFLUOROMETHYLSULFONYL)-3-AZABICYCLO-[3.1.0]-HEXAN-1-YL]-5,6-DIHYDROPYRIDIN-1(2H)-(ISOXAZOL-5
SpectraBase Compound ID Hch7IX08VMZ
InChI InChI=1S/2C22H22F3N3O5S/c2*23-22(24,25)34(31,32)28-13-21(10-17(21)19(28)15-5-3-14(12-29)4-6-15)16-2-1-9-27(11-16)20(30)18-7-8-26-33-18/h2*2-8,17,19,29H,1,9-13H2/t2*17-,19+,21+/m00/s1
InChIKey DROUKDWQTHEUBY-RRMCILSDSA-N
Mol Weight 994.98 g/mol
Molecular Formula C44H44F6N6O10S2
Exact Mass 994.246453 g/mol
Enantiomer InChIKey DROUKDWQTHEUBY-COQWMNJGSA-N

View Spectrum of #61B;MAJOR+MINOR;[(3-[(1S,4S,5R)-4-[4-(HYDROXYMETHYL)-PHENYL]-3-(TRIFLUOROMETHYLSULFONYL)-3-AZABICYCLO-[3.1.0]-HEXAN-1-YL]-5,6-DIHYDROPYRIDIN-1(2H)-(ISOXAZOL-5

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
7-Amino-5-(2-chlorophenyl)-1,3-dimethyl-2,4-dioxo-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]pyrimidine-6-carbonitrile
DI-[6-METHYL-8-ALPHA-(DIETHYLCARBAMOYLAMINO)-ERGOLINE-1-YL]-METHANE
2-(4-Methoxybenzoyl)-3-(4-methylphenyl)-4H-thieno[3,2-c]-chromen-4-one
CYTOCHALASIN_Z_12
9,10-DIHYDRO-YOHIMBINE
(2,7-di-tert-butyl-9H-fluoren-9-yl)(prop-1-en-2-yloxy)bis(2,4,6-tri-tert-butylphenyl)stannane
4H-Pyrano[2, 3-d]pyrimidine-3-carbonitrile, 5,6,7,8-tetrahydro-2-amino-4-(2-fluorophenyl)-6,8-dimethyl-5,7-dioxo-
(9E)-9-(4-fluorobenzylidene)-3,5-bis(4-fluorophenyl)-6,7,8,9-tetrahydro-5H-[1,3]thiazolo[2,3-b]quinazoline
HIIRAGILIDE-NONAACETATE
24-Methylene-5.alpha.-cholest-24(28)-en-3.beta.,6.beta.,15.alpha.,16.beta.,26-pentol
Title Journal or Book Year
Synthesis of skeletally diverse alkaloid-like molecules: exploitation of metathesis substrates assembled from triplets of building blocks Beilstein Journal of Organic Chemistry 2013
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