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Cc1c(C)c2c(c(C)c1O)CC[C@@](C)(CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O2

Cc1c(C)c2c(c(C)c1O)CC[C@@](C)(CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O2
Reaction #55674
α-tocopherol
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #78834
phenolic acids
DOI: 10.6084/m9.figshare.5104873.v1
CCCC1Oc2c(C)c(C)c3c(c2C(CCC)O1)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O3
Reaction #92087
7,9,10-trimethyl-2,4-dipropyl-7-(4,8,12-trimethyl-tridecyl)-4,5,6,7-tetrahydro-1,3,8-trioxa-phenanthrene
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1c(O)c(C)c(C)c2c1CC[C@@](C)(CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O2
Reaction #92088
(R,R,R)-5-butyl-2,7,8-trimethyl-2-(4,8,12-trimethyl-tridecyl)-chroman-6-ol
Ausbeute 105.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1=C(CC[C@](C)(O)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)C(=O)C(C)=C(C)C1=O
Reaction #92090
(R,R,R)-2-allyl-3-(3-hydroxy-3,7,11,15-tetramethyl-hexadecyl)-5,6-dimethyl-[1,4]benzoquinone
Ausbeute 81.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1.CCCCC/C=C\C/C=C\CCCCCCCC(=O)O
Reaction #161066
beta-carotene linoleic
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C)c2c(c(C)c1OC(=O)OCC1OC1(C)CO)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O2
Reaction #273593
DOI: 10.1039/C8SC04228D
Cc1c(C)c2c(c(C)c1O)CC[C@@](C)(CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O2
Reaction #319580
α-tocopherol
Ausbeute 78.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C)c2c(c(C)c1O)CC[C@@](C)(CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O2
Reaction #347022
α-tocopherol
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C)c2c(c(C)c1O)CC[C@@](C)(CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O2.Nc1ccc(C(=O)[O-])cc1
Reaction #412279
alpha-tocopherol 4-aminobenzoate
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1ccc(C(=O)Oc2c(C)c(C)c3c(c2C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O3)nc1
Reaction #413114
dl-α-tocopheryl 5-butylpicolinate
Ausbeute 46.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C)c2c(c(C)c1OC(=O)c1ccc(CCC(Br)CBr)cn1)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O2
Reaction #413115
dl-α-tocopheryl 5-(3,4-dibromobutyl)picolinate
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C)c2c(c(C)c1OC(=O)c1cccnc1)CC[C@@](C)(CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O2
Reaction #459209
dl-α-tocopheryl nicotinate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C)c2c(c(C)c1O)CC[C@@](C)(CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O2
Reaction #463681
title compound
Ausbeute 100.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C)c2c(c(C)c1O)CC[C@@](C)(CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O2
Reaction #463682
title compound
Ausbeute 101.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C)c2c(c(C)c1O)CC[C@@](C)(CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O2
Reaction #463683
title compound
Ausbeute 102.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C)c2c(c(C)c1O)CC[C@@](C)(CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O2
Reaction #463684
title compound
Ausbeute 101.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C)c2c(c(C)c1O)CC[C@@](C)(CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O2
Reaction #463685
title compound
Ausbeute 101.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C)c2c(c(C)c1O)CC[C@@](C)(CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O2
Reaction #463686
title compound
Ausbeute 98.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C)c2c(c(C)c1O)CC[C@@](C)(CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O2
Reaction #463687
title compound
Ausbeute 101.2%DOI: 10.6084/m9.figshare.5104873.v1
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