子结构搜索

9390

CCOC(=O)COc1ccc(CC(=O)Nc2cccc(C3CCC(C(C)(C)C)CC3)c2)cc1OC
Reaction #7170
N-[3-(4-tert-butylcyclohexan-1-yl)phenyl]-4-ethoxycarbonylmethyloxy 3-methoxyphenylacetamide
收率 75.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CC(=O)Nc2cccc(C3CCC(C(C)(C)C)CC3)c2)ccc1OCCO
Reaction #7177
desired compound
收率 50.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](CO)CN1CCc2cc(F)ccc21)O[C@@H](CC1CCCCC1)C(=O)N1CCOCC1
Reaction #43551
title compound
收率 71.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](OCc1ccccc1)[C@H]1CO[C@H](OCCCC2CCCC2)CN1.O=C(O)C(F)(F)F
Reaction #48616
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cccc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](OCCC)CN2)c1
Reaction #49233
title compound
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cccc(C(=O)N(CCC)CCC)c2)C1
Reaction #49234
title compound
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cc(C)cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](OCCC)CN2)c1
Reaction #49240
title compound
收率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cc(C)cc(C(=O)N(CCC)CCC)c2)C1
Reaction #49241
title compound
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1COc2ccc(CNC3CCC(C(=O)c4nc5ccccc5s4)CC3)cc2N1
Reaction #173029
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCCOc1cc(OCCCCc2ccc3cc(OCc4ccccc4)c(OCc4ccccc4)cc3c2)cc(N(CC(=O)OC)CC(=O)OC)c1
Reaction #173808
DOI: 10.1039/C8SC04228D
CCC[Si]1(c2ccccc2)CCC(C2CCC(COc3ccc(OC(F)(F)F)cc3)CC2)CC1
Reaction #176525
DOI: 10.1039/C8SC04228D
CC(NC(=O)C(O)C(CCCCNC(=O)N1CCOCC1)NC(=O)OCC1(Cc2ccccc2)CCCCC1)c1ccccc1
Reaction #185342
DOI: 10.1039/C8SC04228D
CC1CC(C)CC2(C1)CC2C(=O)O
Reaction #202697
DOI: 10.1039/C8SC04228D
CCCCCCCCCC(=O)OC(Cn1ccnc1)c1ccc(Cl)cc1Cl
Reaction #207004
DOI: 10.1039/C8SC04228D
O=C1NC(Cc2cc(F)cc(F)c2)C(C2CC(O)CN2C(c2ccccc2)c2ccccc2)O1
Reaction #212504
DOI: 10.1039/C8SC04228D
CC(NC(=O)C(=O)C(CCCCNC(=O)N1CCOCC1)NC(=O)OCC1(Cc2ccc(F)cc2)CCC1)c1ccccc1
Reaction #212984
DOI: 10.1039/C8SC04228D
N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)[C@H]1CCCCN1C(c1ccccc1)c1ccccc1
Reaction #220121
title compound
收率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N[C@@H](Cc2cc(F)cc(F)c2)[C@@H]([C@H]2C[C@H](O)CN2C(c2ccccc2)c2ccccc2)O1
Reaction #220127
title compound
收率 29.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N[C@@H](Cc2cc(F)cc(F)c2)[C@@H]([C@H]2C[C@H](O)CN2C(c2ccccc2)c2ccccc2)O1
Reaction #220128
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1C(Nc2cnn(C(Cc3ccncc3)C(=O)O)c(=O)c2Br)CC2CC1C2(C)C
Reaction #226559
DOI: 10.1039/C8SC04228D
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