Substructure Search

343186

COc1ccc(C(=O)Nc2cc(CCc3cc(OC)cc(OC)c3)n[nH]2)cc1
Reaction #45006
title compound
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3cccc(OC)c3)n[nH]2)cc(OC)c1
Reaction #45016
title compound
Yield 59.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3ccc(N4CCNCC4)s3)n[nH]2)cc(OC)c1
Reaction #45021
title compound
Yield 13.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(COc2cc(NC(=O)c3ccc(N4CCNCC4)nc3)[nH]n2)cc(OC)c1
Reaction #45033
title compound
Yield 26.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(NC(=O)c2cc(Oc3ccc(C(=O)N4CCC4)cc3F)cc(O[C@@H](C)CO[Si](C)(C)C(C)(C)C)c2)cn1
Reaction #48799
desired compound
Yield 101.6%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1cc(F)c(F)cc1Cl
Reaction #48876
title compound
Yield 96.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)Oc1cc(Oc2cc(F)c(C(=O)N3CCC3)cc2F)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48877
title compound
Yield 31.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO[Si](C)(C)C(C)(C)C)Oc1cc(Oc2ccc(C(=O)N3CCC3)cc2Cl)cc(C(=O)Nc2cnccn2)c1
Reaction #48882
desired compound
Yield 12.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cc(-c2cccc3[nH]ccc23)cc2[nH]ncc12)c1cc2ccccn2n1
Reaction #70522
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)[C@H](C)[C@H]1COC(=O)N1
Reaction #85654
(R)—N-methoxy-N-methyl-2-((S)-2-oxooxazolidin-4-yl)propanamide
Yield 195.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1C(O)CC(O)(C(=O)OCc2ccccc2)OC1C(O)C(O)COC(=O)C(NC(=O)OCc1ccccc1)C(C)C
Reaction #164435
( 1-5 )
Yield 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(C=CC(=O)Cl)C1C(=O)OC(C#N)c1cccc(Oc2ccccc2)c1
Reaction #186453
DOI: 10.1039/C8SC04228D
COCC(O[Si](C)(C)C(C)(C)C)C(=O)Nc1nc(C)ns1
Reaction #188894
DOI: 10.1039/C8SC04228D
COCC(C)Oc1cc(Oc2ccc3c(c2)OCN(C)C3=O)cc(C(=O)Nc2ccn(C(=O)OC(C)(C)C)n2)c1
Reaction #190433
DOI: 10.1039/C8SC04228D
CCCCOc1ccc(CN(C(=O)C=Cc2ccc(C(F)(F)F)cc2)C(Cc2ccccc2)C(=O)N2CCN(Cc3ccccc3)CC2)cc1
Reaction #196013
DOI: 10.1039/C8SC04228D
O=C(Nc1ccn(C(F)F)n1)c1cc(Oc2ccc(C(=O)N3CCC3)nc2)cc(OC2CCOC2)c1
Reaction #228588
DOI: 10.1039/C8SC04228D
COc1ncc(Br)cc1NC(=O)C(C)O
Reaction #238683
DOI: 10.1039/C8SC04228D
COc1cccc2c1c(NS(=O)(=O)c1ccc(Cl)s1)nn2Cc1cccc(CNC(=O)C(C)(C)O)c1
Reaction #244378
DOI: 10.1039/C8SC04228D
CCC(=O)NC1CCC(C(=O)N(C)c2ccc(-c3nc4ccccc4n3C)cc2)C1
Reaction #245899
DOI: 10.1039/C8SC04228D
CN1Cc2ccccc2C12CCN(C(=O)c1c[nH]c3cc(Cl)ccc13)CC2
Reaction #261791
DOI: 10.1039/C8SC04228D
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