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CCCCCCCCCCC=C

C=CCCCC(O)CCCC(CCCc1ccc(C(=O)O)cc1)C(C)=O
Reaction #54880
4-(4-acetyl-8-hydroxytridec-12-en-1-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCCCCCCCC[Si](Cl)(Cl)Cl
Reaction #54910
13-tetradecenyl trichlorosilane
Ausbeute 30.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCCCCCCCC[Si](Cl)(Cl)Cl
Reaction #55313
13-tetradecenyl trichlorosilane
Ausbeute 30.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCCC(O)C=C[C@H]1CCC(=O)[C@@H]1CCCCCCC(=O)O
Reaction #55566
9-keto-15-hydroxy-19-methyl-prosta-13,18-dienoic acid
Ausbeute 91.5%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)C(=O)O[C@H]1C[C@H](O)C=C2C=C[C@H](C)[C@H](CC[C@@H](O)C[C@@H](O)CC(=O)O)[C@H]21
Reaction #59804
Pravastatin
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(N)C2CC3CC1CC(O)(C3)C2
Reaction #66725
4-allyl-4-amino-adamantan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
CCCC1(N)C2CC3CC1CC(O)(C3)C2
Reaction #66726
title compound
Ausbeute 76.9%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCC(O)CCCC(CCCc1ccc(C(=O)O)cc1)C(C)=O
Reaction #75247
4-(4-acetyl-8-hydroxytridec-12-en-1-yl)benzoic acid
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
CCCC1=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 #92091
(R,R,R)-2-(3-hydroxy-3,7,11,15-tetramethyl-hexadecyl)-5,6-dimethyl-3-propyl-[1,4]benzoquinone
Ausbeute 80.0%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)=CC1=O
Reaction #92092
(R,R,R)-2-allyl-3-(3-hydroxy-3,7,11,15-tetramethyl-hexadecyl)-5-methyl-[1,4]benzoquinone
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #92093
oil
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC1=C(CC[C@](C)(O)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)C(=O)C(C)=CC1=O
Reaction #92094
(R,R,R)-3-(3-hydroxy-3,7,11,15-tetramethyl-hexadecyl)-5-methyl-2-propyl-[1,4]benzoquinone
Ausbeute 45.2%DOI: 10.6084/m9.figshare.5104873.v1
OC1(CCCCCC2CC3CC2C2C4C=CC(C4)C32)CCCC1
Reaction #173335
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCC(O)C(O)C(N)(CO)CO
Reaction #179810
DOI: 10.1039/C8SC04228D
C=CCCCCCCCCCCCC[Si](Cl)(Cl)Cl
Reaction #193910
DOI: 10.1039/C8SC04228D
CC(CC#N)C1CCC2C(=CBr)CCCC21C
Reaction #203698
DOI: 10.1039/C8SC04228D
CCCCCCCCC=CCCCCCCCCCCC
Reaction #203867
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCC(O)C1=CC(=O)OC1OC
Reaction #205927
DOI: 10.1039/C8SC04228D
Cc1ccccc1CSC1CCC2C3CCC4=CC(=O)C=CC4(C)C3C(=O)CC12C
Reaction #206005
DOI: 10.1039/C8SC04228D
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