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(1S,5S,6S)-(-)-2-OXA-BICYCLO-[3.1.0]-HEX-3-ENE-3,6-DICARBOXYLIC-ACID-6-ETHYLESTER-3-METHYLESTER

Compound with spectra: 3 NMR, and 2 MS (GC)

(1S,5S,6S)-(-)-2-OXA-BICYCLO-[3.1.0]-HEX-3-ENE-3,6-DICARBOXYLIC-ACID-6-ETHYLESTER-3-METHYLESTER
SpectraBase Compound ID K7pXy7MwBQT
InChI InChI=1S/C10H12O5/c1-3-14-10(12)7-5-4-6(9(11)13-2)15-8(5)7/h4-5,7-8H,3H2,1-2H3/t5-,7-,8-/m0/s1
InChIKey RZWKTOFPJZAYJO-GEVIPFJHSA-N
Mol Weight 212.2 g/mol
Molecular Formula C10H12O5
Exact Mass 212.068473 g/mol
Enantiomer InChIKey RZWKTOFPJZAYJO-LPBLVHEISA-N

View Spectrum of (1S,5S,6S)-(-)-2-OXA-BICYCLO-[3.1.0]-HEX-3-ENE-3,6-DICARBOXYLIC-ACID-6-ETHYLESTER-3-METHYLESTER

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum QF-9-264-8

View Spectrum of (1S,5S,6S)-(-)-2-OXA-BICYCLO-[3.1.0]-HEX-3-ENE-3,6-DICARBOXYLIC-ACID-6-ETHYLESTER-3-METHYLESTER

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum KD-14-770-6

View Spectrum of (1S,5S,6S)-(-)-2-OXA-BICYCLO-[3.1.0]-HEX-3-ENE-3,6-DICARBOXYLIC-ACID-6-ETHYLESTER-3-METHYLESTER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (1S,5S,6S)-(-)-2-OXA-BICYCLO-[3.1.0]-HEX-3-ENE-3,6-DICARBOXYLIC-ACID-6-ETHYLESTER-3-METHYLESTER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (1S,5S,6S)-(-)-2-OXA-BICYCLO-[3.1.0]-HEX-3-ENE-3,6-DICARBOXYLIC-ACID-6-ETHYLESTER-3-METHYLESTER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (1S,5S,6S)-6-ETHYL-3-METHYL-2-OXABICYCLO-[3.1.0]-HEX-3-ENE-3,6-DICARBOXYLATE
  • 6-ETHYL-3-METHYL-(1S,5S,6S)-(-)-2-OXA-BICYCLO-[3.1.0]-HEX-3-ENE-3,6-DICARBOXYLATE
  • (1S,5S,6S)-(-)-2-Oxabicyclo[3.1.0]hex-3-ene-3,6-dicarboxylic acid 6-ethyl -3-methyl ester
(4R,5S,6R)-4,5,6,7-Tetrahydroxy-pentylidenecyclohexane-spiro-2'-(1',3'-dioxolan)-4'-one
(E)-Diethyl2-(1-oxaspiro[5.6]dodecan-2-ylmethyl)-2-(4-hydroxybut-2-enyl)malonate
(E)-diethyl2-(6-oxaspiro[4.5]decan-7-ylmethyl)-2-(4-hydroxybut-2-enyl)malonate
8-t-Butyl-1,4-dioxa-spiro[4.5]decane-6-carboxylic acid, ethyl ester
Diisopropyl (2R,3S)-2-Allyl-3-(tert-butyldimethylsiloxy)succinate
2-Hydroxy-1-ethyl-2-methyl-4-methylidene-cyclopentanecarboxylic acid, ethyl ester
50521-99-8
9-HYDROXY-10-OXO-BIOPHENOTHRIN
(2R,4R)-[2-TERT.-BUTYL-4-(3-METHYLBUT-2-ENYL)-5-OXO-1,3-DIOXOLAN-4-YL]-ACETIC-ACID
(2R,3R)-2-allyl-3-[tert-butyl(dimethyl)silyl]oxy-succinic acid diethyl ester
Title Journal or Book Year
Enantioselective Synthesis of Furo[2,3-b]furans, a Spongiane Diterpenoid Substructure Organic Letters 2005
Facile Asymmetric Synthesis of the Core Nuclei of Xanthanolides, Guaianolides, and Eudesmanolides Organic Letters 2003
Enantioselective Synthesis of (−)-Roccellaric Acid Organic Letters 2001
Other Resources
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