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1-O-BUTYRYL-(1S,6S,7R,8R,8AR)-1,6,7,8-TETRAHYDROXYOCTAHYDROINDOLIZINE;1-O-BUTYRYLCASTANOSPERMINE

Compound with spectra: 1 NMR

1-O-BUTYRYL-(1S,6S,7R,8R,8AR)-1,6,7,8-TETRAHYDROXYOCTAHYDROINDOLIZINE;1-O-BUTYRYLCASTANOSPERMINE
SpectraBase Compound ID AWawl3zrNKL
InChI InChI=1S/C12H21NO5/c1-2-3-9(15)18-8-4-5-13-6-7(14)11(16)12(17)10(8)13/h7-8,10-12,14,16-17H,2-6H2,1H3/t7-,8-,10+,11+,12+/m0/s1
InChIKey MIANLSLDYWCVDY-VWNXEWBOSA-N
Mol Weight 259.3 g/mol
Molecular Formula C12H21NO5
Exact Mass 259.141973 g/mol
Enantiomer InChIKey MIANLSLDYWCVDY-PPJKGSGRSA-N

View Spectrum of 1-O-BUTYRYL-(1S,6S,7R,8R,8AR)-1,6,7,8-TETRAHYDROXYOCTAHYDROINDOLIZINE;1-O-BUTYRYLCASTANOSPERMINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(1R,6S,7R,8R,8aR)-1-Butyryloxy-6,7,8-trihydroxyindolizidine[(-)-1-O-Butyryl-1-epicastanospermine]
[1S,6S,7R,8R,8aR)-2-O-Butanoyl-6,7,8-trihydroxyoctahydroindolizine] 2-O-Butanoylcastanospermine
1-O-OCTANOYL-(1S,6S,7R,8R,8AR)-1,6,7,8-TETRAHYDROXYOCTAHYDROINDOLIZINE;1-O-OCTANOYLCASTANOSPERMINE
DETOXIN-A1
2a,3,4,5,7,8,8a,8b-Octahydro-3-hydroxy-2H-furo[4,3,2-h,i]indolizin-2-one
(+)-7,9-O,O'-(3,3-Pentamethyleneglutaryl)-heliotridine
Spiro[cyclohexane-1,4'-[4H][1,6]dioxacycloundecino[2,3,4-gh]pyrrolizine]-2',6'(3'H,5'H)-dione, 8',10',12',13',13'a,13'b-hexahydro-, [13'aS-(13'aR*,13'bS*)]-
(+)-7,9-O,O'-(3,3-Dimethylglutaryl)heliotridine
(+)-1,9-O,O'-(3,3-Dimethylglutaryl)-heliotridine
Spiro[cyclopentane-1,4'-[4H][1,6]dioxacycloundecino[2,3,4-gh]pyrrolizine]-2',6'(3'H,5'H)-dione, 8',10',12',13',13'a,13'b-hexahydro-, [13'aS-(13'aR*,13'bS*)]-
Title Journal or Book Year
Enzyme-catalyzed regioselective acylation of castanospermine Journal of the American Chemical Society 1990

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