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#8;ETHYL-[(1''S,2''R,4''R)-N,N-DIISOPROPYLBORNAN-10''-SULFONAMIDE-2''-YL]-2-[(1'-ALPHA-ETHYL-1',2',3',4',6',7',12',12B'-ALPHA-OCTAHYDROINDOLO-[2',3'-A]-QUINOLIZIN-

Compound with spectra: 2 NMR

#8;ETHYL-[(1''S,2''R,4''R)-N,N-DIISOPROPYLBORNAN-10''-SULFONAMIDE-2''-YL]-2-[(1'-ALPHA-ETHYL-1',2',3',4',6',7',12',12B'-ALPHA-OCTAHYDROINDOLO-[2',3'-A]-QUINOLIZIN-
SpectraBase Compound ID 7J7ZvVlh5XL
InChI InChI=1S/C39H59N3O6S/c1-9-38(18-13-20-41-21-17-29-28-14-11-12-15-31(28)40-33(29)34(38)41)23-30(35(43)47-10-2)36(44)48-32-22-27-16-19-39(32,37(27,7)8)24-49(45,46)42(25(3)4)26(5)6/h11-12,14-15,25-27,30,32,34,40H,9-10,13,16-24H2,1-8H3/t27-,30?,32-,34-,38+,39-/m1/s1
InChIKey SKOMNXIAHMZXJV-AOLXHMHBSA-N
Mol Weight 698.0 g/mol
Molecular Formula C39H59N3O6S
Exact Mass 697.412458 g/mol
Enantiomer InChIKey SKOMNXIAHMZXJV-MMJBNQQZSA-N

View Spectrum of #8;ETHYL-[(1''S,2''R,4''R)-N,N-DIISOPROPYLBORNAN-10''-SULFONAMIDE-2''-YL]-2-[(1'-ALPHA-ETHYL-1',2',3',4',6',7',12',12B'-ALPHA-OCTAHYDROINDOLO-[2',3'-A]-QUINOLIZIN-

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

View Spectrum of #8;ETHYL-[(1''S,2''R,4''R)-N,N-DIISOPROPYLBORNAN-10''-SULFONAMIDE-2''-YL]-2-[(1'-ALPHA-ETHYL-1',2',3',4',6',7',12',12B'-ALPHA-OCTAHYDROINDOLO-[2',3'-A]-QUINOLIZIN-

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Ethyl {(1"S,2"R,4"R)-N,N-diisopropylbornan-10"-sulfonamid-2"-yl} 2-{(1'.alpha.-ethyl-1',2',3',4',6',7',12',12b'.alpha.octahydroindolo[2',3'-a]quinolizin-1'.beta.-yl)methyl}malonate diasteromer
Title Journal or Book Year
Synthesis of Vinca Alkaloids and Related Compounds LXXXVIII. Highly Enantioselective Synthesis of (+)-Vincamine HETEROCYCLES 1997
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