Busqueda de Subestructura

1517

CN1CC(CCCl)Oc2ccc([N+](=O)[O-])cc2C1=S
Reaction #4920
yellow crystals
Rendimiento 173.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=Cc2ccccn2)CCc2ccc([N+](=O)[O-])cc21
Reaction #7155
7-nitro-1-oxo-2-(2-pyridylmethylidene)-1,2,3,4-tetrahydronaphthalene
Rendimiento 19.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N)cc(C(=O)O)c1
Reaction #42269
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Reaction #42276
ethyl acetate hexanes
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C(=C1SCS1)c1ccncc1)c1cccc([N+](=O)[O-])c1
Reaction #66348
yellow solid
Rendimiento 76.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccco1)c1cc([N+](=O)[O-])ccc1Cl
Reaction #77242
title compound
Rendimiento 78.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C=O)c([N+](=O)[O-])c1
Reaction #78641
Methyl 4-formyl-3-nitrobenzoate
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)c1cc(N(C(=O)OC(C)(C)C)c2ccc(CO)cc2[N+](=O)[O-])ncn1
Reaction #86462
crude residue
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(N(C(=O)OC(C)(C)C)C(=O)N(C)c2cc(N(C(=O)OC(C)(C)C)c3ccc(C(=O)O)cc3[N+](=O)[O-])ncn2)c1Cl
Reaction #86465
title compound
Rendimiento 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(N(C(=O)OC(C)(C)C)C(=O)N(C)c2cc(N(C(=O)OC(C)(C)C)c3ccc(C(=O)N4CCN(C)CC4)cc3[N+](=O)[O-])ncn2)c1Cl
Reaction #86466
title compound
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(C(=O)C3CC3)cc2[N+](=O)[O-])CC1
Reaction #157043
tert-butyl 4-(4-(cyclopropanecarbonyl)-2-nitrophenyl)piperazine-1-carboxylate
Rendimiento 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCN(c2ccc(C(=O)C3CC3)cc2[N+](=O)[O-])CC1
Reaction #157044
tert-butyl 1-(4-(cyclopropanecarbonyl)-2-nitrophenyl)piperidin-4-ylcarbamate
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCCN(c2ccc(C(=O)C3CC3)cc2[N+](=O)[O-])C1
Reaction #157045
tert-butyl 1-(4-(cyclopropanecarbonyl)-2-nitrophenyl)piperidin-3-ylcarbamate
Rendimiento 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NNC(=O)c1cccc([N+](=O)[O-])c1)c1cccc(Cl)c1
Reaction #158525
N′1-(3-chlorobenzoyl)-3-nitrobenzene-1-carbohydrazide
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(-c2nnc(-c3cccc(Cl)c3)o2)c1
Reaction #158526
[2-(3-chlorophenyl)-1,3,4-oxadiazol-5-yl]-3-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2c(c1)C(O)CCC2
Reaction #161269
7-nitro-1,2,3,4-tetrahydro-naphthalen-1-ol
Rendimiento 80.4%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2c(c1)C(=NO)CCC2
Reaction #161271
7-nitro-3,4-dihydro-2H-naphthalen-1-one oxime
Rendimiento 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCNc1ccc(C(=O)O)cc1[N+](=O)[O-]
Reaction #161441
title compound
Rendimiento 80.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCNc1ccc(C(=O)O)cc1N
Reaction #161442
title compound
Rendimiento 80.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NNC(=O)c1cccc([N+](=O)[O-])c1)c1cccc(Cl)c1
Reaction #163634
N′1-(3-chlorobenzoyl)-3-nitrobenzene-1-carbohydrazide
DOI: 10.6084/m9.figshare.5104873.v1
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