Busqueda de Subestructura

755432

Cl.Clc1ccc(C23CNCC2C3)cc1Cl
Reaction #11492
(−)-1-(3,4-Dichlorophenyl)-3-azabicyclo[3.1.0]hexane HCl
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)n1c(=O)c(I)cn(CCCN2CC3CC3(c3ccc(Cl)cc3)C2)c1=O
Reaction #40986
1-{3-[1-(4-chlorophenyl)-3-azabicyclo[3.1.0]hex-3-yl]propyl}-5-iodo-3-(phenylcarbonyl)-2,4(1H,3H)-pyrimidinedione
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(=O)n(CCCN2CC3CC3(c3ccc(Cl)cc3)C2)cc1I
Reaction #40987
title compound
Rendimiento 83.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Clc1ccc(C23CNCC2C3)cc1
Reaction #94551
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Cl)cc1)N1CC2CC2(c2ccc(Cl)cc2)C1
Reaction #94555
3-p-chlorobenzoyl-1-(p-chlorophenyl)-3-azabicyclo[3.1.0]hexane
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(CN2CC3CC3(c3ccc(Cl)cc3)C2)cc1
Reaction #94556
3-(p-Chlorobenzyl)-1-(p-chlorophenyl)-3-azabicyclo[3.1.0]hexane
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CC2CC2(c2ccc(Cl)cc2)C1)C12CC3CC(CC(C3)C1)C2
Reaction #94557
3-(1-adamantylcarbonyl)-1-(p-chlorophenyl)-3-azabicyclo[3.1.0]hexane
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1F)N1CC2CC2(c2ccc(Cl)cc2)C1
Reaction #94559
3-(o-fluorobenzoyl)-1-(p-chlorophenyl)-3-azabicyclo[3.1.0]hexane
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Fc1ccccc1CN1CC2CC2(c2ccc(Cl)cc2)C1
Reaction #94560
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CC2CC2(c2ccc(Cl)cc2)C1
Reaction #94572
3-acetyl-1-(p-chlorophenyl)-3-azabicyclo[3.1.0]hexane
DOI: 10.6084/m9.figshare.5104873.v1
CCC1NCC2(c3ccc(Cl)cc3)CC12
Reaction #94576
pink semisolid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CC2CC2(c2ccc(Cl)c(Cl)c2)C1
Reaction #175937
DOI: 10.1039/C8SC04228D
O=CN1CC2CC2(c2ccc(Cl)cc2)C1
Reaction #204405
DOI: 10.1039/C8SC04228D
O=C(c1cccc(F)c1)N1CC2CC2(c2ccc(Cl)cc2)C1
Reaction #208694
DOI: 10.1039/C8SC04228D
O=C(c1ccc(Cl)cc1)N1CC2CC2(c2ccc(Cl)cc2)C1
Reaction #227318
DOI: 10.1039/C8SC04228D
Clc1ccc(CN2CC3CC3(c3ccc(Cl)cc3)C2)cc1
Reaction #227921
DOI: 10.1039/C8SC04228D
O=C(c1ccc(Cl)cc1)N1CC2CC2(c2ccc(Cl)cc2)C1
Reaction #244068
DOI: 10.1039/C8SC04228D
O=C(N1CC2CC2(c2ccc(Cl)cc2)C1)C12CC3CC(CC(C3)C1)C2
Reaction #255523
DOI: 10.1039/C8SC04228D
O=C(c1ccc(F)cc1)N1CC2CC2(c2ccc(Cl)cc2)C1
Reaction #274090
DOI: 10.1039/C8SC04228D
Cl.Clc1ccc(C23CNCC2C3)cc1
Reaction #311456
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
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