部分構造検索

15058

O=Cc1ccccc1Oc1ccc(Cl)cc1[N+](=O)[O-]
Reaction #49958
2-(2-nitro-4-chloro-phenoxy)benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #64550
desired material
収率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccccc1Oc1ccc(Cl)cc1[N+](=O)[O-]
Reaction #65631
2-(2-nitro-4-chloro-phenoxy)benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1cc(C(=O)N2Cc3ccc(-c4ccc(N5CCN(C(=O)OC(C)(C)C)CC5)cc4)cc3C2)c(OCc2ccccc2)cc1OCc1ccccc1
Reaction #69721
4-{4-[2-(2,4-bis-benzyloxy-5-isopropenyl-benzoyl)-2,3-dihydro-1H-isoindol-5-yl]-phenyl}piperazine-1-carboxylic acid tert-butyl ester
収率 26.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O.CC(=O)O.CN1CCN([C@H]2CC[C@H](n3cc(-c4ccc(Oc5ccccc5)c(C=O)c4)c4c(N)ncnc43)CC2)CC1
Reaction #79869
trans-5-{4-amino-7-[4-(4-methylpiperazino)cyclohexyl]-7H-pyrrolo[2,3-d]pyrimidin-5-yl}-2-phenoxybenzaldehyde bisacetate
収率 102.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(NC(=O)c2ccccc2Cl)ccc1C(=O)N1CCCC(OCCNC(C)=N)c2cc(Cl)ccc21.Cl
Reaction #83033
5-[2-(1-iminoethyl)aminoethoxy]-7-chloro-1-[2-methoxy-4-(2-chlorobenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzo-azepine hydrochloride
収率 69.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1c(OCc2ccc(S(C)(=O)=O)cc2Cl)cccc1C(=O)c1cn([Si](C(C)C)(C(C)C)C(C)C)c2ncccc12
Reaction #175134
DOI: 10.1039/C8SC04228D
CCOc1c(OCc2ccc(S(C)(=O)=O)cc2Cl)cccc1C(=O)c1c[nH]c2ncccc12
Reaction #188151
DOI: 10.1039/C8SC04228D
O=C(Nc1cc(C(F)(F)F)ccc1Cl)c1cc(Cl)ccc1OC(=O)N1CCOCC1
Reaction #199319
DOI: 10.1039/C8SC04228D
C=CCOc1cc(OCC=C)c(C(=O)c2ccc(S(C)(=O)=O)cc2)c(CC(=O)N(CCOC)CCOC)c1CC
Reaction #207640
DOI: 10.1039/C8SC04228D
O=C(O)c1ccccc1Oc1cc(Cl)ccc1[N+](=O)[O-]
Reaction #209254
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(Oc2c(C(N)=O)cc(N)cc2C(N)=O)CC1
Reaction #211876
DOI: 10.1039/C8SC04228D
CC(Oc1ccc(S(C)(=O)=O)cc1C(=O)N1Cc2ccc(-c3ccncc3)nc2C1)C(F)(F)F
Reaction #221904
DOI: 10.1039/C8SC04228D
Cc1cccc(C(=O)NC2(C(=O)O)Cc3c(C)sc(C)c3C2)c1OC(C)C
Reaction #225054
DOI: 10.1039/C8SC04228D
CC(Oc1ccc(S(C)(=O)=O)cc1C(=O)N1Cc2cnc(N3CCOCC3)cc2C1)C(F)(F)F
Reaction #227391
DOI: 10.1039/C8SC04228D
COc1cc2c(cc1OC)C(C)(C)CN(C(=O)c1cc(S(C)(=O)=O)ccc1OC(C)C)C2
Reaction #233821
DOI: 10.1039/C8SC04228D
CC(Oc1ccc(S(C)(=O)=O)cc1C(=O)N1Cc2cc(I)c(C(F)(F)F)cc2C1)C(F)(F)F
Reaction #234335
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(Oc2ccc(N)cc2C(N)=O)CC1
Reaction #246566
DOI: 10.1039/C8SC04228D
COc1ccc(-c2cn(S(=O)(=O)c3ccc(C)cc3)c3ncccc23)cc1C#N
Reaction #250540
DOI: 10.1039/C8SC04228D
CC1(C)CCC(CN2CCN(c3ccc(C(=O)NS(=O)(=O)c4ccc(NC5CN(C6CCOCC6)C5)c([N+](=O)[O-])c4)c(Oc4cnc5[nH]ccc5c4)c3)CC2)=C(c2ccc(Cl)cc2)C1
Reaction #259218
DOI: 10.1039/C8SC04228D
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