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(+)-(1R,5AS,7S,7AR,7BR)-1,7-DIHYDROXY-6-OXAOCTAHYDRO-2H-CYCLOPENTA-[GH]-PYRROLIZIN-2-ONE

Compound with spectra: 1 NMR, and 2 MS (GC)

(+)-(1R,5AS,7S,7AR,7BR)-1,7-DIHYDROXY-6-OXAOCTAHYDRO-2H-CYCLOPENTA-[GH]-PYRROLIZIN-2-ONE
SpectraBase Compound ID KYIr43A6wxR
InChI InChI=1S/C8H11NO4/c10-6-4-5-3(13-8(4)12)1-2-9(5)7(6)11/h3-6,8,10,12H,1-2H2/t3-,4-,5+,6-,8+/m1/s1
InChIKey QHJDXFDMYJJOJT-WVISBBDJSA-N
Mol Weight 185.18 g/mol
Molecular Formula C8H11NO4
Exact Mass 185.068808 g/mol
Enantiomer InChIKey QHJDXFDMYJJOJT-UQGZVRACSA-N

View Spectrum of (+)-(1R,5AS,7S,7AR,7BR)-1,7-DIHYDROXY-6-OXAOCTAHYDRO-2H-CYCLOPENTA-[GH]-PYRROLIZIN-2-ONE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum C-118-8276-26

View Spectrum of (+)-(1R,5AS,7S,7AR,7BR)-1,7-DIHYDROXY-6-OXAOCTAHYDRO-2H-CYCLOPENTA-[GH]-PYRROLIZIN-2-ONE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum C-118-8276-26

View Spectrum of (+)-(1R,5AS,7S,7AR,7BR)-1,7-DIHYDROXY-6-OXAOCTAHYDRO-2H-CYCLOPENTA-[GH]-PYRROLIZIN-2-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
  • (1R,5aS,7S,7aR,7bR)-1,7-Dihydroxy-6-oxaoctahydro-2H-cyclopenta[gh]pyrrolizin-2-one
REL-(1R,5AR,7S,7AR,7BR)-1,7-DIHYDROXY-6-OXAOCTAHYDRO-2H-CYCLOPENTA-[GH]-PYRROLIZIN-2-ONE
3,3-Dimethoxydecahydroazepino[3,2,1-hi]indol-2-one
(1S,2R,8R,8aR)-8-(Benzyloxy)-1,2-(isopropylidenedioxy)indolizine
9-BENZYL-5-OXA-9-AZATRICYCLO-[5.2.1.0(4,8)]-DECAN-6-ONE
9-Benzyl-5-oxa-9-azatricyclo[5.2.1.0(4,8)]decane-6-one
1(R)-acetoxy-7(S)-(acetoxymethyl)-7a(S)-hexahydro-6(S)-iodo-3H-pyrrolizin-3-one
(RS)-2-(N-((1RS,2SR,3RS,4SR)-3-(Hydroxymethyl)-7-oxa-bicyclo[2.2.1]hept-5-en-2-yl)-N-methylamino)-n-benzyl-4-methylpentanamide
(3AR,4R,9AS,9BS)-4-(METHOXYMETHOXY)-2,2-DIMETHYLOCTAHYDRO-[1,3]-DIOXOLO-[4,5-G]-INDOLIZIDINE
(1S,2R,7R,8S,8aR)-(-)-1,2-O-Isopropylidene-7,8-dihydroxyindolizidine
Allyl-2-deoxy-2-hexanoylamino-3,4,6-tri-O-benzyl-b-d-allopyranoside
Title Journal or Book Year
Tandem [4 + 2]/[3 + 2] Cycloadditions of Nitroalkenes. 9. Synthesis of (−)-Rosmarinecine Journal of the American Chemical Society 1996
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