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(7S,20S)-(+)-RHAZIDIGENIN

Compound with spectra: 1 NMR

(7S,20S)-(+)-RHAZIDIGENIN
SpectraBase Compound ID GnKjgWnVXcB
InChI InChI=1S/C19H26N2O/c1-2-18-9-5-12-21(14-18)13-11-19(22)15-6-3-4-7-16(15)20-17(19)8-10-18/h3-4,6-7,22H,2,5,8-14H2,1H3/t18-,19-/m1/s1
InChIKey QNNPSMFAKZAUMA-RTBURBONSA-N
Mol Weight 298.43 g/mol
Molecular Formula C19H26N2O
Exact Mass 298.204513 g/mol
Enantiomer InChIKey QNNPSMFAKZAUMA-OALUTQOASA-N

View Spectrum of (7S,20S)-(+)-RHAZIDIGENIN

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3:DMSO-D6
Rhazidigenine
10a-phenyl-6,7,8,9,10,10a-hexahydrocyclohepta[b]indole
(1R*,2R*)-2'-Ethylspiro[2-methylcyclohexan-1,3'-3'H-indole]
(1R*,2S*)-2'-Ethylspiro[2-methylcyclohexan-1,3'-3'H-indole]
2-(2-Methoxyphenyl)spiro[3,1-benzoxazine-4,1'-cyclopentane]
2-(4a-hydroxy-1-(3,4,5-trimethoxyphenyl)octahydro-2(1H)-isoquinolinyl)acetamide
12H-4-AZATRICYCLO[4.3.1.1^3^,^8]UNDECANO[5,4-b]QUINAZOLIN-12-ONE
Biperiden AC
3-(p-Tolylsulfonyl)-5-tert-butyl-1,2,3-benzoxathiazole 2,2-Dioxide
Indapamide -2H 3ME
Title Journal or Book Year
Synthesis of vinca alakaloids and realated compounds98. Oxidation with dimethyldioxirane of compounds containing the aspidospermane and quebrachamine ring system. A simple synthesis of (7S,20S)-(+)-rhazidigenine and (2R,7S,20S)-(+)-rhazidine Journal of Heterocyclic Chemistry 2002
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