子结构搜索

1305677

C[Si](C)(C)CCOCn1nccc1C(=O)c1ccccc1N
Reaction #2426
mixture
收率 49.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)O)c([N+](=O)[O-])c1
Reaction #3207
benzoic acid
收率 91.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N)c1C(=O)O
Reaction #3208
benzoic acid
收率 100.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(=O)c1ccccc1[N+](=O)[O-])Nc1ccc(Oc2ncc(Br)cn2)c(Cl)c1
Reaction #4609
desired product
收率 84.5%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Oc2ncc(Cl)cn2)c(Cl)c1
Reaction #4610
3-chloro-4-(5-chloro-2-pyrimidinyloxy)aniline
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc(OCc3cccc(F)c3)ccc2c(=O)n1CC(N)=O
Reaction #7724
title compound
收率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc(OCc3cccc(F)c3)ccc2c(=O)n1CC(N)=O
Reaction #7725
title compound
收率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)C2=C(O)C3CCC(C3)C2=O)c([N+](=O)[O-])c1
Reaction #52570
4-hydroxy-3-(4-methanesulfonyl-2-nitrobenzoyl)-bicyclo[3.2.1]oct-3-en-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(O)cc1[N+](=O)[O-]
Reaction #57966
4-hydroxy-2-nitrobenzoic acid
收率 54.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([N+](=O)[O-])c(CO)c1
Reaction #61074
title compound
收率 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)N2CCCC2CO)c([N+](=O)[O-])cc1OC
Reaction #62260
(4,5-Dimethoxy-2-nitro-phenyl)-(2-hydroxymethyl-pyrrolidin-1-yl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([N+](=O)[O-])c(C(=O)Nc2ccc(Cl)cn2)c1
Reaction #67625
2-nitro-N-(5-chloro-pyridin-2-yl)-5-methoxy-benzamide
收率 88.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)cc(N)c1[N+](=O)[O-]
Reaction #72779
desired product
收率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CCOCC2)cc(N)c1[N+](=O)[O-]
Reaction #72780
desired product
收率 46.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CCOCC2)cc2nc(C)[nH]c12
Reaction #72781
desired product
收率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CCOCC2)cc(N)c1N
Reaction #72799
desired product
收率 80.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CCOCC2)cc(N)c1N
Reaction #72825
crude product
收率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(O)ccc(C=NNc2ccc(C3=NNC(=O)C[C@H]3C)cc2)c1[N+](=O)[O-]
Reaction #75545
(R)-6-{4-[N′-(4-Hydroxy-3-methoxy-2-nitro-benzylidene)-hydrazino]-phenyl }-5-methyl-4,5-dihydro-2H-pyridazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc([N+](=O)[O-])c1C=O
Reaction #77957
2-methyl-6-nitrobenzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([N+](=O)[O-])c(CO)c1
Reaction #84113
product
收率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
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