子结构搜索

857521

CC(=O)Nc1cccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2)c1
Reaction #2589
title compound
收率 74.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccc(F)cc2)c1
Reaction #2591
title compound
收率 98.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCCc2ccc(C(=O)N[C@@H](Cc3cc(F)cc(F)c3)[C@H](O)CNCc3cccc(CC)c3)cc21
Reaction #42522
1-butyl-N-{(1S,2R)-1-(3,5-difluorobenzyl)-3-[(3-ethylbenzyl)amino]-2-hydroxypropyl}-1,2,3,4-tetrahydroquinoline-7-carboxamide
收率 41.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)c3cccc(N4CC5CCC(C4)N5C(C)c4ccccc4)c3C2=O)cc1OC
Reaction #70602
title Compound 32
收率 38.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([N+](=O)[O-])cc1C(=O)NCC1CC1
Reaction #75725
N-cyclopropylmethyl-2-methoxy-5-nitrobenzamide
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)c2cccc(N)c2C1=O
Reaction #76501
product
收率 181.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1Nc1ccncc1)N1CCCCC1
Reaction #93167
1-[5-nitro-2-(4-pyridinylamino)benzoyl]piperidine
DOI: 10.6084/m9.figshare.5104873.v1
CNC1=NN(C(=O)c2cccc([N+](=O)[O-])c2)C(C)(C)S1
Reaction #96008
5,5-Dimethyl-2-methylamino-4-(3-nitrobenzoyl)-4,5-dihydro-1,3,4-thiadiazole
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(NC(=O)c2ccc(OC)c(N)c2)c1
Reaction #176487
DOI: 10.1039/C8SC04228D
Nc1ccc(C(=O)Nc2ccc(C(F)(F)F)nc2)cc1[N+](=O)[O-]
Reaction #176546
DOI: 10.1039/C8SC04228D
CCNC(=O)c1cc([N+](=O)[O-])ccc1Oc1cncc(Cl)c1
Reaction #176857
DOI: 10.1039/C8SC04228D
Cc1ccc(C(=O)NC2CC2)cc1-n1cnc2ccc(OCC(C)(O)CO)cc2c1=O
Reaction #179757
DOI: 10.1039/C8SC04228D
CC(=O)Oc1cc(C(=O)NCc2ccccc2)cc([N+](=O)[O-])c1OC(C)=O
Reaction #181166
DOI: 10.1039/C8SC04228D
O=C(Cl)CN1C(=O)c2ccc([N+](=O)[O-])cc2C1=O
Reaction #184111
DOI: 10.1039/C8SC04228D
CCN(CC)C(=O)c1ccc([N+](=O)[O-])c(N)c1
Reaction #184327
DOI: 10.1039/C8SC04228D
COc1ccc(C(=O)Nc2cc(NC(=O)c3cccc(N(C)C)c3)c(F)cc2Cl)cc1OC
Reaction #185173
DOI: 10.1039/C8SC04228D
CN1C(=O)c2ccc(N)cc2C1=O
Reaction #186279
DOI: 10.1039/C8SC04228D
C[n+]1ccc(Nc2cccc(C(=O)Nc3ccc([N+](=O)[O-])cc3)c2)cc1
Reaction #188672
DOI: 10.1039/C8SC04228D
Cc1ccc(C(=O)NC2CC2)cc1-n1cnc2ccc(OCCNS(C)(=O)=O)cc2c1=O
Reaction #189400
DOI: 10.1039/C8SC04228D
CN1C(=O)c2cccc(N)c2C1=O
Reaction #189999
DOI: 10.1039/C8SC04228D
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