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3-(TERT.-BUTYL)-8,9-DIMETHYL-(1RS,2SR,6RS,7SR,8SR,9RS)-10-OXA-3,4,5-TRIAZATRICYCLO-[5.2.1.0(2,6)]-DEC-4-ENE-3,8,9-TRICARBOXYLATE

Compound with spectra: 1 NMR

3-(TERT.-BUTYL)-8,9-DIMETHYL-(1RS,2SR,6RS,7SR,8SR,9RS)-10-OXA-3,4,5-TRIAZATRICYCLO-[5.2.1.0(2,6)]-DEC-4-ENE-3,8,9-TRICARBOXYLATE
SpectraBase Compound ID KHgRgxno5TH
InChI InChI=1S/C15H21N3O7/c1-15(2,3)25-14(21)18-9-8(16-17-18)10-6(12(19)22-4)7(11(9)24-10)13(20)23-5/h6-11H,1-5H3/t6-,7-,8-,9+,10+,11-/m1/s1
InChIKey ZBMPCDVBQNJYJK-UPMLMMEUSA-N
Mol Weight 355.35 g/mol
Molecular Formula C15H21N3O7
Exact Mass 355.13795 g/mol
Enantiomer InChIKey ZBMPCDVBQNJYJK-UDLFHZNPSA-N

View Spectrum of 3-(TERT.-BUTYL)-8,9-DIMETHYL-(1RS,2SR,6RS,7SR,8SR,9RS)-10-OXA-3,4,5-TRIAZATRICYCLO-[5.2.1.0(2,6)]-DEC-4-ENE-3,8,9-TRICARBOXYLATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
3-ETHYL-8,9-DIMETHYL-(1RS,2SR,6RS,7SR,8SR,9RS)-10-OXA-3,4,5-TRIAZATRICYCLO-[5.2.1.0(2,6)]-DEC-4-ENE-3,8,9-TRICARBOXYLATE
ethyl 2-[3-(2-furoyl)-4-hydroxy-5-oxo-2-phenyl-2,5-dihydro-1H-pyrrol-1-yl]-4-methyl-1,3-thiazole-5-carboxylate
CINNABARAMIDE_G
methyl 2-[2-(4-bromophenyl)-4-hydroxy-5-oxo-3-(2-thienylcarbonyl)-2,5-dihydro-1H-pyrrol-1-yl]-4-methyl-1,3-thiazole-5-carboxylate
5-(7-Chloro-3,3-dimethyl-1-oxo-2,3,4,9-tetrahydro-1H-xanthen-9-yl)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione
BHQKBUUYUQPHNG-KPJGAVQNSA-N
(t-butyl) (2R*,3'R*,12bR*)-(+-)-1,2,6,7,12,12b-hexahydro-2-(tetrahydro-2'-furanon-3'-yl)-indolo[2,3-a]quinolizine-3-carboxylate
(1aR,5R,5aS)-5a-[3-(tert-Butyldimethylsilyloxy)phenyl]-5-methoxy-5-[(Z)-6-trimethylsilyl-3-hexene-1,5-diynyl]-perhydrobenzo[b]oxiren-1a-carbaldehyde
Methyl 2'-methoxy-6'-oxo-7'-phenylsulfanylspiro[cyclopropane-1,8'-bicyclo[3.2.1]oct-2'-ene]-1'-carboxylate
(1S,3R,5R,6R,8R)-3-ACETOXYMETHYL-5-BENZYLOXY-6-BENZYLOXYMETHYL-8-(THYMIN-1-YL)-2,7-DIOXABICYCLO-[3.3.0]-OCTANE
Title Journal or Book Year
Acid-Promoted Rearrangements ofN-Substituted 8-Oxa-3-azatricyclo[3.2.1.02?4] octane-6,7-dicarboxylates: Remote Substituent Effects on the Regioselectivity of theN-Acylaziridine/Dihydrooxazone Rearrangement Helvetica Chimica Acta 1990
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