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[3R,6R,7S,(8E),10S,11S,(12E)]-MACROLACTONE

Compound with spectra: 1 NMR

[3R,6R,7S,(8E),10S,11S,(12E)]-MACROLACTONE
SpectraBase Compound ID EdYMFng2BLx
InChI InChI=1S/C28H49IO8Si/c1-20-11-12-24(35-22(3)30)28(7,34-19-33-16-15-32-8)14-13-23(37-38(9,10)27(4,5)6)17-25(31)36-26(20)21(2)18-29/h11-12,18,20,23-24,26H,13-17,19H2,1-10H3/b12-11+,21-18+/t20-,23+,24-,26-,28+/m0/s1
InChIKey PEVNQIJGZJRDLP-JXKBNNTPSA-N
Mol Weight 668.7 g/mol
Molecular Formula C28H49IO8Si
Exact Mass 668.22414 g/mol
Enantiomer InChIKey PEVNQIJGZJRDLP-FDNFCTBCSA-N

View Spectrum of [3R,6R,7S,(8E),10S,11S,(12E)]-MACROLACTONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
[3R,6R,7R,(8E),10S,11S,(12E)]-MACROLACTONE
PLADIENOLIDE-E
PLADIENOLIDE-D
NK30424A
5.alpha.,7.alpha.,11,16-Tetrahydroxytetranor-prost-9 trans-enoic acid methyl ester t-butyldimethylsilyl ether
(1R,2S,3S,4R,6R,7S)-1,4-DI-O-TERT.-BUTYLDIMETHYLSILYL-2,3-O-METHYLETHYLIDENE-6,7-O-SULFONYL-CYCLOOCTANE-1,2,3,4,6,7-HEXOL
(1S,2S,3S,4S,6R,7S)-1,4-DI-O-TERT.-BUTYLDIMETHYLSILYL-2,3-O-METHYLETHYLIDENE-6,7-O-SULFONYL-CYCLOOCTANE-1,2,3,4,6,7-HEXOL
2'-methyl-5,6,7,8-tetrahydrospiro[chroman-2,1'-cyclohexan]-2'-ol, acetate
[2S-(1E,2.alpha.,3.alpha.,5.alpha.)]-[3-(acetyloxy)-2hydroxy-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-methylcyclohexylidene]acetic acid ethyl ester
(4S,5R)-4-{(1S,2S,3R)-2-(tert-Butyl-dimethyl-silanyloxy)-3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-1-methoxy-pent-4-enyl}-2,2,5-trimethyl-[1,3]dioxolane
1D-1-O-(TERT.-BUTYLDIPHENYLSILYL)-2,3,6-O-TRIS-(METHOXYMETHYLENE)-MYO-INOSITOL
Title Journal or Book Year
Synthesis of Pladienolide B and Its 7-Epimer with Insights into the Role of the Allylic Acetate European Journal of Organic Chemistry 2013
[3R,6R,7S,(8E),10S,11S,(12E)]-MACROLACTONE
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