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C=COCCCC

CCCCOC(=O)CCCCCSC1=C(OC(=O)CCC)C[C@@H](O)[C@@H]1/C=C/[C@@H](O)C[C@H](C)CCCC
Reaction #3126
butyl (11R,12S,13E,15S,17R)-9-butyryloxy-11,15-dihydroxy-17,20-dimethyl-7-thiaprosta-8,13-dienoate
Rendimiento 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCSC1=C(OC(=O)CCC)C[C@@H](O)[C@@H]1/C=C/[C@@H](O)CCCCC
Reaction #3129
(11R,12S,13E,15S)-9-butyryloxy-11,15-dihydroxy-7-thiaprosta-8,13-diene
Rendimiento 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@@H](/C=C/[C@@H]1C(SCCCCCC(N)=O)=C(OC(=O)CCC)C[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C
Reaction #3133
(11R,12S,13E,15S)-9-butyryloxy-11,15-bis(tert-butyldimethylsiloxy)-7-thiaprosta-8,13-dienamide
Rendimiento 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H](O)/C=C/[C@@H]1C(SCCCCCC(N)=O)=C(OC(=O)CCC)C[C@H]1O
Reaction #3134
(11R,12S,13E,15S)-9-butyryloxy-11,15-dihydroxy-7-thiaprosta-8,13-dienamide
Rendimiento 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)OC1=Cc2c(cc(OC)c3c(=O)c4cc5ccccc5nc4n(C)c23)OC1(C)C
Reaction #46320
6-Methoxy-3,3,14-trimethyl-7-oxo-7,14-dihydro-3H-benzo[b]chromeno[6,5-g][1,8]naphthyridin-2-yl butyrate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC1=C(OCCCC)CC1
Reaction #48529
3,4-dibutoxy-3-cyclobutene
Rendimiento 12.2%DOI: 10.6084/m9.figshare.5104873.v1
CC[NH+](C(C)C)C(C)C
Reaction #52568
ethyldiisopropyl-ammonium
DOI: 10.6084/m9.figshare.5104873.v1
CC[NH+](CC)CC.O=C1C=C(O)C2CCC1C2
Reaction #52569
4-hydroxybicyclo[3.2.1]oct-3-en-2-one triethylammonium salt
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)C2=C(O)C3CCC(C3)C2=O)c([N+](=O)[O-])c1
Reaction #52570
4-hydroxy-3-(4-methanesulfonyl-2-nitrobenzoyl)-bicyclo[3.2.1]oct-3-en-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)C2=C(O)C3CCC(C3)C2=O)c([N+](=O)[O-])c1
Reaction #52571
4-hydroxy-3-(4-methanesulfonyl-2-nitrobenzoyl)-bicyclo[3.2.1]oct-3-en-2-one
Rendimiento 44.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C(F)(F)F)ccc1C(=O)OC1=CC(=O)C2CCC1C2
Reaction #52572
2-methyl-6-trifluoromethylnicotinic acid 4-oxobicyclo[3.2.1]oct-2-en-2-yl ester
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)OC2=CC(=O)C3CCC2C3)c(Cl)c1Cl
Reaction #52573
2,3-Dichloro-4-methanesulfonylbenzoic acid 4-oxobicyclo[3.2.1]oct-2-en-2-yl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[N-]C(C)C.[Li+]
Reaction #53622
LDA
DOI: 10.6084/m9.figshare.5104873.v1
CCC1=C2CC(N(C)C)C3=C2C(=CN1S(=O)(=O)c1ccccc1)C=COC3
Reaction #53623
titled compound
Rendimiento 98.4%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=C2CC(N(C)C)C3=C2C(=CN1)C=COC3
Reaction #53624
titled compound
Rendimiento 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)OC(C)(C)C)[C@H](C)O
Reaction #64079
t-butyl (3S)-2-methyl-3-hydroxybutanoate
Rendimiento 43.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C(=O)OC(C)(C)C)[C@H](C)O
Reaction #64085
t-butyl (3S )-2-ethyl-3-hydroxybutanoate
Rendimiento 66.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC(C(=O)OC(C)(C)C)[C@H](C)O
Reaction #64086
t-butyl (3S)-2-allyl-3-hydroxybutanoate
Rendimiento 45.3%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](O)C(C)C(=O)OC
Reaction #64087
methyl (3S)-2-methyl-3-hydroxypentanoate
Rendimiento 77.8%DOI: 10.6084/m9.figshare.5104873.v1
CCc1sc(-c2ccc(Cl)cc2)nc1C1=C(OC(=O)C2CC2)C2C3CCC(O3)C2C1=O
Reaction #69966
cyclopropanecarboxylic acid-4-[2-(4-chloro-phenyl)-5-ethyl-thiazol-4-yl]-5-oxo-10-oxa-tricyclo[5.2.1.0*2,6*]dec-3-en-3-yl ester
Rendimiento 124.3%DOI: 10.6084/m9.figshare.5104873.v1
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