部分構造検索

897622

COc1cc(Br)c2oc3c(c2c1)C1C(=O)NC(=O)C1C(c1ccccc1Cl)C3
Reaction #11248
7-Bromo-4-(2-chlorophenyl)-9-methoxy-3a,4,5,10c-tetrahydro-1H-[1]benzofuro[3,2-e]isoindole-1,3(2H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Br)c2oc3cc(-c4ccccc4Cl)c4c(c3c2c1)C(=O)NC4=O
Reaction #11249
dibenzofuran
収率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1oc2cc3c(cc2c1-c1ccccc1)OCO3
Reaction #74903
5,6-methylenedioxy-2-nitro-3-phenylbenzofuran
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)oc2ccc(Oc3nc(OC)cc(OC)n3)c(C(=O)O)c12
Reaction #80273
desired compound
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)oc2ccc(Oc3nc(OC)cc(OC)n3)c(C(=O)OCOC(=O)C(C)(C)C)c12
Reaction #80274
desired compound
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)nc(Oc2ccc3oc(C(F)(F)F)c(C(=O)c4ccccc4)c3c2C(=O)[O-])n1.[Na+]
Reaction #80278
desired compound
収率 40.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C)oc2ccc(Oc3nc(OC)nc(OC)n3)c(C(=O)OCc3ccccc3)c12
Reaction #80279
desired compound
収率 109.7%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)c1c(Oc2nc(OC)cc(OC)n2)ccc2oc(C)c(C(=O)N(C)C)c12
Reaction #80283
desired compound
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)nc(Oc2ccc3oc(C)c(C(=O)N(C)C)c3c2C(=O)O)n1
Reaction #80284
desired compound
収率 80.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=S)c1c(C)oc2ccc(Oc3nc(OC)cc(OC)n3)c(C(=O)O)c12
Reaction #80285
desired compound
収率 91.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(Nc2ccc(C(=O)N(C)CCC(=O)O)cc2)C2CCCCC2)oc2ccc(OCc3ccccc3)cc12
Reaction #179329
DOI: 10.1039/C8SC04228D
CCOC(=O)CCNC(=O)c1ccc(NC(CCCCOC)c2oc3ccc(OC)cc3c2C)cc1
Reaction #183196
DOI: 10.1039/C8SC04228D
COCCCCC(Nc1ccc(C(=O)O)cc1)c1oc2ccc(OC)cc2c1C
Reaction #188257
DOI: 10.1039/C8SC04228D
CNC(=O)c1c(-c2ccc(Oc3ccc(F)cc3)cc2)oc2ccc(O)c(F)c12
Reaction #189656
DOI: 10.1039/C8SC04228D
COc1ccc2oc(C(CC(C)C)Nc3ccc(C(=O)NCCC(=O)O)cc3)c(C)c2c1
Reaction #194369
DOI: 10.1039/C8SC04228D
COc1ccc2oc(C(=O)C(C)(C)C)c(CC(=O)N3CCC4CCCCC4C3)c2c1
Reaction #195064
DOI: 10.1039/C8SC04228D
Cc1c(C(Nc2ccc(C(=O)NCCC(=O)O)cc2)C2CCCCC2)oc2ccc(OCc3ccc(Cl)nc3)cc12
Reaction #196611
DOI: 10.1039/C8SC04228D
Cc1c(C(Nc2ccc(C(=O)N(C)CCC(=O)O)cc2)C2CCCCC2)oc2ccc(OCc3cccnc3)cc12
Reaction #196704
DOI: 10.1039/C8SC04228D
CCN(CC)CCOc1ccc(-c2oc3ccc(OC)cc3c2C(=O)c2cc(C)cc(C)c2)cc1
Reaction #197827
DOI: 10.1039/C8SC04228D
CCN(CCC(C)(C)C)C(=O)Cc1c(C(=O)C(C)(C)C)oc2ccc(OC)cc12
Reaction #198724
DOI: 10.1039/C8SC04228D
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