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(2E,4S,5S,15R)-4,5-DIHYDROXYHEXADEC-2-EN-15-OLIDE

Compound with spectra: 1 NMR

(2E,4S,5S,15R)-4,5-DIHYDROXYHEXADEC-2-EN-15-OLIDE
SpectraBase Compound ID 55EIsEcVWT5
InChI InChI=1S/C16H28O4/c1-13-9-7-5-3-2-4-6-8-10-14(17)15(18)11-12-16(19)20-13/h11-15,17-18H,2-10H2,1H3/b12-11+/t13-,14+,15+/m1/s1
InChIKey QYHZVIDSYPZOAI-RQOPNEMTSA-N
Mol Weight 284.4 g/mol
Molecular Formula C16H28O4
Exact Mass 284.198759 g/mol
Enantiomer InChIKey QYHZVIDSYPZOAI-XMFCPKQUSA-N

View Spectrum of (2E,4S,5S,15R)-4,5-DIHYDROXYHEXADEC-2-EN-15-OLIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3:DMSO-D6
(2E,4R,5S,15R)-4,5-DIHYDROXYHEXADEC-2-EN-15-OLIDE
Cladospolide B
Cladospolide A
ISO-CLADOSPOLIDE
CHLORIOLIDE
OFFICINOIC_ACID_B
4-Methyl-6-undecyl-5,6-dihydropyran-2-one
4-Methyl-6-nonyl-5,6-dihydro-2H-pyran-2-one
(+/-)-(ERITHRO)-(2E)-N-4,5-DIHYDROXY-DEC-2-ENOYL-PIPERIDINE
(+/-)-(THREO)-(2E)-N-4,5-DIHYDROXY-DEC-2-ENOYL-PIPERIDINE
Title Journal or Book Year
Synthese des Makrolid-Antibiotikums (−)-A26771B mit Photolactonisierung als Schlüsselreaktion und Computersimulation als effektive Optimierungshilfe Helvetica Chimica Acta 1991

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