Busqueda de Subestructura

CCCCCCCCCCCCCCCCC(=O)O

CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@](O)(C(=O)OCCl)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1502
3-(Chloromethoxycarbonyl) Cholesterol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCC[C@@H](C[C@@H]1OC(=O)[C@H]1CC)OC(=O)[C@H](CC(C)C)NC=O
Reaction #6163
N-formyl-(S)-leucine (S)-1-[[(2S,3S)-3-ethyl-4-oxo-2-oxetanyl]methyl]octadecyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C/C(=C\c1csc(C)n1)[C@@H]1C[C@@H]2O[C@]2(C)CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1
Reaction #42642
epothilone B
DOI: 10.6084/m9.figshare.5104873.v1
C/C(=C\c1csc(C)n1)[C@@H]1C[C@@H]2O[C@]2(C)CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1
Reaction #53255
epothilone B
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCC[C@H]1C2OCCOC2C[C@@H]1CCC(=O)CCC=C(C)C
Reaction #55563
9-ethylenedioxy-15-keto-19-methyl-prost-18-enoic acid, methyl ester
Rendimiento 88.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCC[C@H]1C2OCCOC2C[C@@H]1CCC(=O)CCC=C(C)C
Reaction #55564
9-ethylenedioxy-15-keto-19-methyl-prost-18-enoic acid, methyl ester
Rendimiento 94.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)C=C[C@@]43C)[C@@H]1CC(C(C(=O)O)C(=O)O)[C@@H]2C(=O)CO
Reaction #63002
21-acetoxy-16α-methoxycarbonyl-11β-hydroxy-3,20-dioxo-1,4-pregnadiene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #65344
CHOLESTEROL
DOI: 10.6084/m9.figshare.5104873.v1
C=CS(=O)(=O)C(CCCCCCC(=O)O)CCCC(O)CCCCC
Reaction #93919
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H](O)CCCC(CCCCCCC(=O)O)S(C)(=O)=O
Reaction #93925
product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(CC[C@H]1CCC(=O)[C@@H]1CCCCCCC(=O)OCC)OC(C)(C)C
Reaction #95267
desired product
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)CC[C@H]1CCC(=O)[C@@H]1CCCCCCC(=O)OCC
Reaction #95268
15-hydroxy-9-oxoprostanoic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(CCCCCCCCCCC(=O)O)O[Si](C)(C)C(C)(C)C
Reaction #186793
DOI: 10.1039/C8SC04228D
CC(CC(O[SiH](C)C)C(=O)O)C1CC=C2C3=C(CCC21C)C1(C)CCC(C(C)(C)C)C(C)(C)C1CC3
Reaction #197427
DOI: 10.1039/C8SC04228D
CC(C)=CCCC(=O)CCC1CC2OCCOC2C1CCCCCCC(=O)O
Reaction #211114
DOI: 10.1039/C8SC04228D
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #215679
CHOLESTEROL
DOI: 10.6084/m9.figshare.5104873.v1
NCCCCCCCCCCCCCCCCC(=O)O
Reaction #216838
17-aminoheptadecanoic acid
Rendimiento 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCCCCCCCCCCCCCCN1C(=O)c2ccccc2C1=O
Reaction #216839
17-phthalimidoheptadecanoic acid
Rendimiento 142.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)N(OC2CCCCC2)C(C)(C)C1
Reaction #220835
title compound
Rendimiento 846.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCCCCCCCCCCCCCCCCCc1c(C)cc(OC)c(OC)c1O
Reaction #223477
DOI: 10.1039/C8SC04228D
Página 1Siguiente