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#22;(2S,2AS,4AS,5R,6S,7AR,7BR)-6-[(1R,2S)-(2-PHENYLCYCLOHEXYL)-OXY]-OCTAHYDRO-7B-METHYL-1,7-DIOXA-7A-AZACYCLOPENT-[CD]-INDANE-2-CARBOXYLIC-ACID-METHYLESTER

Compound with spectra: 1 NMR

#22;(2S,2AS,4AS,5R,6S,7AR,7BR)-6-[(1R,2S)-(2-PHENYLCYCLOHEXYL)-OXY]-OCTAHYDRO-7B-METHYL-1,7-DIOXA-7A-AZACYCLOPENT-[CD]-INDANE-2-CARBOXYLIC-ACID-METHYLESTER
SpectraBase Compound ID BRIcn6lPO1o
InChI InChI=1S/C24H33NO5/c1-15-18-13-14-19-21(22(26)27-3)29-25(24(18,19)2)30-23(15)28-20-12-8-7-11-17(20)16-9-5-4-6-10-16/h4-6,9-10,15,17-21,23H,7-8,11-14H2,1-3H3/t15?,17?,18-,19+,20?,21?,23?,24+/m1/s1
InChIKey PUOUDLLLLMYDKL-CLMWWCROSA-N
Mol Weight 415.5 g/mol
Molecular Formula C24H33NO5
Exact Mass 415.235873 g/mol
Enantiomer InChIKey PUOUDLLLLMYDKL-LXSFMQRMSA-N

View Spectrum of #22;(2S,2AS,4AS,5R,6S,7AR,7BR)-6-[(1R,2S)-(2-PHENYLCYCLOHEXYL)-OXY]-OCTAHYDRO-7B-METHYL-1,7-DIOXA-7A-AZACYCLOPENT-[CD]-INDANE-2-CARBOXYLIC-ACID-METHYLESTER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
#21;(2S,2AS,4AS,5S,6S,7AR,7BR)-6-[(1R,2S)-(2-PHENYLCYCLOHEXYL)-OXY]-OCTAHYDRO-7B-METHYL-1,7-DIOXA-7A-AZACYCLOPENT-[CD]-INDANE-2-CARBOXYLIC-ACID-METHYLESTER
REL-(1R,6S,7S,8R,9S)-6-CYCLOHEXYLOXY-6,9-DIMETHYL-8-PHENYL-4-AZA-3,5-DIOXATRICYCLO-[5.3.1.0(4,9)]-DECANE
2-CHLORO-6-CYCLOHEXYLAMINO-9-(BETA-D-2,3,5-O-TRIACETYL-RIBOFURANOSYL)-PURINE
1H-pyrazolo[3,4-b]pyridine, 3-cyclopropyl-6-(2,5-dimethoxyphenyl)-1-(4-methoxyphenyl)-4-(trifluoromethyl)-
(22R,23R)-3.beta.-Acetoxy-24-methyl-22,23-epoxy-5.alpha.-cholestan-6-one
7-Benzoyl-3-methyl-pyrrolo[1,2-c]pyrimidine-5,6-dicarboxylic acid dimethyl ester
1-Benzyl 5-Methyl 3-hydroxy-3-phenyl-1-tosylpyrrolidine-1,5-dicarboxylate
2-{[3-(4-methylphenyl)-4-oxo-3,4,5,6,7,8-hexahydro[1]benzothieno[2,3-d]pyrimidin-2-yl]sulfanyl}-N'-[(E)-(2,4,5-trimethoxyphenyl)methylidene]acetohydrazide
(22S,23R,24R)-3.beta.-Acetoxy-22-hydroxy-23-bromo-24-methyl-5.alpha.-cholestan-6-one
(22S,23R,24R)-3.beta.-Acetoxy-22-bromo-23-hydroxy-24-methyl-5.alpha.-cholestan-6-one
Title Journal or Book Year
Tandem inter [4+2]/intra [3+2]nitroalkene cycloadditions. 5. Origin of the Lewis acid dependent reversal of stereoselectivity The Journal of Organic Chemistry 1993
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