Busqueda de Subestructura

O=C(Cl)c1cccc2ccccc12

Cl.O=C(NCCCSc1ccncc1)c1cccc2ccccc12
Reaction #6198
desired compound
Rendimiento 74.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc2c(cc1NC(=O)c1cccc3ccccc13)OCO2
Reaction #66926
150
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NC(=O)c2cccc3ccccc23)sc1C(=O)NCc1ccccc1
Reaction #73625
title compound
Rendimiento 12.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cccc2ccccc12)c1c[nH]c2ccccc12
Reaction #84199
3-(1-naphthoyl)-1H-Indole
Rendimiento 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]cc(C(=O)c3cccc4ccccc34)c2c1
Reaction #84202
5-methoxy-3-(1-naphthoyl)-1H-indole
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccc(Br)c2ccccc12
Reaction #159002
4-bromonaphthalene-1-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=CC(=O)c1ccc(Br)c2ccccc12
Reaction #159003
1-(4-bromonaphthalen-1-yl)-2-diazoethanone
DOI: 10.6084/m9.figshare.5104873.v1
COCCn1c(C)c(C)s/c1=N\C(=O)c1ccc2c3c(cccc13)CC2
Reaction #165627
title compound
Rendimiento 22.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccc(Br)c2ccccc12
Reaction #166954
4-bromonaphthalene-1-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=CC(=O)c1ccc(Br)c2ccccc12
Reaction #166955
1-(4-bromonaphthalen-1-yl)-2-diazoethanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc(C(F)(F)F)c1)c1cccc2cc(Oc3ccnc(Cl)n3)ccc12
Reaction #173682
DOI: 10.1039/C8SC04228D
CC(C)C(=O)Nc1cccc(C2CCN(CCC(OC(=O)c3cccc4ccccc34)c3ccccc3)CC2)c1
Reaction #177938
DOI: 10.1039/C8SC04228D
O=C(c1cccc2ccccc12)c1nc(CCN2CCOCC2)n2ccccc12
Reaction #180106
DOI: 10.1039/C8SC04228D
CC1(C)NC(=O)N(C(=O)c2cccc3ccccc23)C1=O
Reaction #188150
DOI: 10.1039/C8SC04228D
O=C(Cl)c1cccc2cc(Oc3ncnc4[nH]ccc34)ccc12
Reaction #191067
DOI: 10.1039/C8SC04228D
O=C(c1cccc2ccccc12)N1CC(CN2CCC(c3ccc(F)cc3)CC2)C(C2CC2)C1
Reaction #206291
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(Oc2ccc(N(Cc3ccc4ccc(C#N)cc4c3)C(=O)c3cccc4ccccc34)cc2)CC1
Reaction #208710
DOI: 10.1039/C8SC04228D
CCOc1ccc2ccccc2c1C(=O)n1cc(-c2ccc(OC)c(OC)c2)c2cccnc21
Reaction #208807
DOI: 10.1039/C8SC04228D
O=C(NC(Cc1ccc(C(F)(F)F)cc1)C(O)c1ccc(F)cc1)c1cccc2ccccc12
Reaction #211803
DOI: 10.1039/C8SC04228D
CN(C(=O)c1cccc2ccccc12)[C@@H]1CN(C2CCCCC2)C[C@H]1O.Cl
Reaction #214097
Trans-N-(1-cyclohexyl-4-hydroxypyrrolidin-3-yl)-N-methyl-1-naphthalenecarboxamide Hydrochloride
Rendimiento 56.0%DOI: 10.6084/m9.figshare.5104873.v1
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