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317646

COC(=O)CCCCCCCC=Cc1ccc(Cl)cc1
Reaction #5353
10-(4-chlorophenyl)-dec-9-enoic acid methyl ester
Ausbeute 13.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCCCCCC=Cc1ccc(Cl)cc1
Reaction #5354
10-(4-chlorophenyl)dec-9-enoic acid
Ausbeute 103.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC[C@H]1C[C@H]1CCCCCCCC(=O)O
Reaction #5364
cis-8-(2 -octylcyclopropyl) octanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7423
final solution
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1CCCC2CC(CC)OC12O
Reaction #40887
desired title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC/C=C\CCCCCCCC(=O)OCC
Reaction #42009
ethyl oleate
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC/C=C\CCCCCCCC(=O)OCC
Reaction #42010
ethyl oleate
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC/C=C\CCCCCCCC(=O)OCCCCC
Reaction #42011
pentyl oleate
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCCCCCCO
Reaction #48891
methyl 11-hydroxyundecanoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #55608
methyl-4-androstene-3-one-17-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=O)O
Reaction #55612
4-androsten-3-one-17β-carboxylic acid
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCN(C)C.C=CC(N)=O
Reaction #56109
Acrylamide DMAEMA
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #66028
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #66029
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #66030
sucrose
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC=CC/C=C/CCCCCCCC(=O)Oc1ccc(-c2ccc(C=CC(=O)OC(C)(C)C)cc2)cc1C12CC3CC(CC(C3)C1)C2
Reaction #70002
(E)-Octadeca-9,12-dienoic acid 3-adamantan-1-yl-4′-(2-tert-butoxycarbonylvinyl)biphenyl-4-yl ester
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC=CC/C=C/CCCCCCCC(=O)Oc1ccc(-c2ccc(C=CC(=O)O)cc2)cc1C12CC3CC(CC(C3)C1)C2
Reaction #70003
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(O)C1CCCCCC=C1Br
Reaction #74254
17
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(O)C1C#CCCCCC1
Reaction #74255
cyclooct-1-yn-3-glycolic acid
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CC/C=C\CC1(C(=O)OC)C(O)CCC1CC(=O)OC
Reaction #74829
compound ( 1-b )
DOI: 10.6084/m9.figshare.5104873.v1
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