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(1R*,3R*,6R*,7R*,8R*)-3-(TERT.-BUTYLDIMETHYLSILOXY)-5-(ISOPROPYL)-6-FORMYL-2-OXA-BICYCLO-[6.4.0]-DODEC-4-ENE-3-CARBOXYLIC-ACID-METHYLESTER

Compound with spectra: 1 NMR

(1R*,3R*,6R*,7R*,8R*)-3-(TERT.-BUTYLDIMETHYLSILOXY)-5-(ISOPROPYL)-6-FORMYL-2-OXA-BICYCLO-[6.4.0]-DODEC-4-ENE-3-CARBOXYLIC-ACID-METHYLESTER
SpectraBase Compound ID CC7E2SL9Fq6
InChI InChI=1S/2C23H40O5Si/c2*1-15(2)17-13-20(28-29(7,8)23(3,4)5)21(22(25)26-6)27-19-12-10-9-11-16(19)18(17)14-24/h2*13-19,21H,9-12H2,1-8H3/b2*20-13+/t2*16-,17+,18+,19+,21-/m00/s1
InChIKey CXCOJZDHBSFNIV-ZFMSKPKTSA-N
Mol Weight 849.3 g/mol
Molecular Formula C46H80O10Si2
Exact Mass 848.529002 g/mol
Enantiomer InChIKey CXCOJZDHBSFNIV-VTQPISDBSA-N

View Spectrum of (1R*,3R*,6R*,7R*,8R*)-3-(TERT.-BUTYLDIMETHYLSILOXY)-5-(ISOPROPYL)-6-FORMYL-2-OXA-BICYCLO-[6.4.0]-DODEC-4-ENE-3-CARBOXYLIC-ACID-METHYLESTER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
8-(TERT.-BUTYLDIMETHYLSILOXY)-6-TERT.-BUTYL-10-HYDROXY-2-OXABICYCLO-[3.3.2]-DEC-7-EN-9-ONE
6-EPI-TANNUNOLIDE-B
3,6-Methanobenzofuran-8-carboxylic acid, 7-(acetyloxy)octahydro-2-oxo-, methyl ester, (3.alpha.,3a.beta.,6.alpha.,7.alpha.,7a.beta.,8R*)-(.+-.)-
ENDO-5-ACETOXY-EXO-3-METHOXYCARBONYLBICYCLO-[2.2.2]-OCTANE-2,6-CARBOLACTONE
8-(TERT.-BUTYLDIMETHYLSILOXY)-6-DIMETHYLPHENYLSILYL-2-OXABICYCLO-[3.3.2]-DEC-7-EN-9-ONE
1,2-ANHYDRIDO-4,5-DIHYDRONIVEUSIN A
NIVEUSIN A,1,2-ANHYDRIDO-4,5-DIHYDRO
OSZDTSWIYQLVST-MURVHARLSA-N
JCXABYACWXHFQQ-VDKZLKBHSA-N
1-BETA-[6-CHLORO-2-[[BIS-(DIMETHYLAMINO)-PHOSPHORYL]-OXY]-PYRIDIN-3-YL]-1,2-DIDEOXY-2,3-DIDEHYDRO-3-O-(TERT.-BUTYLDIMETHYLSILYL)-D-RIBOFURANOSIDE
Title Journal or Book Year
Stereoselective Construction of Eight-Membered Oxygen Heterocycles by Brook Rearrangement-Mediated [3 + 4] Annulation Organic Letters 2004
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