子结构搜索

CCCCCCCCCCC(C)O

CCCCCCC(O)CCCCCCCCCCCCC(O)C[N+](C)(C)CC(C)O.[Br-]
Reaction #1203
title compound
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCC(O)CNCCO
Reaction #1204
title compound
收率 74.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCC(O)CN(C)CCO
Reaction #1205
title compound
收率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(O)CCCCCCCCCCC(=O)NCCNCCO
Reaction #1215
title compound
收率 737.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC(O)C(O)CNCc1ccccc1
Reaction #1217
title compound
收率 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC[C@H](CC(=O)OC)OCc1ccccc1
Reaction #5717
methyl (R)-3-(benzyloxy)-tetradecanoate
收率 112.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(C(=O)O)C(O)CC(CCCCC)OCc1ccccc1
Reaction #5723
rac-(2RS,3RS,5SR)-5-benzyloxy-2-hexyl-3-hydroxy-decanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC1CC(=O)[C@@H](CCCCCC)C(=O)O1
Reaction #6154
tetrahydro-3-hexyl-4-oxo-(R)-6-undecyl-2H-pyran-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC[C@@H]1C[C@H](O)[C@H](CCCCCC)C(=O)O1
Reaction #6155
(3S,4S,6R)-tetrahydro-3-hexyl-4-hydroxy-6-undecyl-2H-pyran-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC[C@@H]1C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](CCCCCC)C(=O)O1
Reaction #6156
(3S,4S,6R)-tetrahydro-3-hexyl-4-[(t-butyldimethylsilyl)oxy]-6-undecyl-2H-pyran-2-one
收率 63.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC[C@@H](C[C@@H]1OC(=O)[C@H]1CCCCCCCCCC)OC(=O)[C@H](CC(C)C)NC=O
Reaction #6161
N-formyl-L-leucine (S)-1-[[(2S,3S)-3-decyl-4-oxo-2-oxetanyl]methyl]-4-pentenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC(O)C(=O)N[C@@H](CCCC)CCC(=O)O
Reaction #48240
(4S)-4-[(2-Hydroxydodecanoyl)amino]octanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC(O)CC(=O)OCc1ccccc1
Reaction #53260
benzyl 3-hydroxymyristate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCC(O)CC(=O)OCc1ccccc1
Reaction #53263
benzyl 3-hydroxyhexadecanoate
DOI: 10.6084/m9.figshare.5104873.v1
C1=CCCCCCC2OC2CCCCCC1
Reaction #63431
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CC[C@H](O)C/C1=C/C=C1\CCC[C@]2(C)[C@@H]([C@H](C)CCCC(C)(C)O)CC[C@@H]12
Reaction #68718
calcifediol
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CC[C@H](O)C/C1=C/C=C1\CCC[C@]2(C)[C@@H]([C@H](C)CCCC(C)(C)O)CC[C@@H]12
Reaction #68719
calcifediol
DOI: 10.6084/m9.figshare.5104873.v1
OC1(CC2CO2)CCCCCCCCCCC1
Reaction #69930
alcohol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCC(O)CNCCN1CCN=C(C)CC1=O
Reaction #95949
4-(2-hydroxytetradecyl)aminoethyl-7-methyl-3,6-dihydro-2H-1,4-diazepin-5-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCC(O)CNCCN1CCN=C(C)CC1=O
Reaction #95950
4-(2-hydroxyhexadecyl)aminoethyl-7-methyl-3,6-dihydro-2H-1,4-diazepin-5-one
DOI: 10.6084/m9.figshare.5104873.v1
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