子结构搜索

1250728

COc1ccc(C2=CCC(C)(C)CC2)c([N+](=O)[O-])c1
Reaction #60410
1-(4,4-Dimethylcyclohex-1-enyl)-4-methoxy-2-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCC1(CC)CC=C(c2ccc(OC)cc2[N+](=O)[O-])CC1
Reaction #60419
1-(4,4-Diethylcyclohex-1-enyl)-4-methoxy-2-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
COC1CCN(c2ccc([N+](=O)[O-])c(C3=CC(C)(C)CC(C)(C)C3)c2)CC1
Reaction #60426
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1CCN(c2ccc([N+](=O)[O-])c(C3=CCC4(CCCCC4)CC3)c2)CC1
Reaction #60428
title compound
收率 111.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(N3CCOCC3)cc2C2=CCC3(CC2)CC3)CC1
Reaction #60452
title compound
收率 90.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc([N+](=O)[O-])c1C1=CC(C)(C)CC(C)(C)C1
Reaction #60467
title compound
收率 99.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([N+](=O)[O-])c(C2=CC(C)(C)CC(C)(C)C2)c1
Reaction #60491
title compound
收率 34.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C2=CC(C)(C)CC(C)(C)C2)c([N+](=O)[O-])cc1OC
Reaction #60497
title compound
收率 85.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(c2cc([N+](=O)[O-])ccc2N2CCN(C(=O)OC(C)(C)C)CC2)CC(C)(C)C1
Reaction #60502
title compound
收率 14.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(c2c(F)cccc2[N+](=O)[O-])CC(C)(C)C1
Reaction #60514
title compound
收率 81.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(c2ccc(F)cc2C2CCN(C(=O)OC(C)(C)C)CC2)CC(C)(C)C1
Reaction #60544
title compound
收率 48.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC=C(c2ccc3cc(O)ccc3n2)CC1
Reaction #84074
methyl 4-(6-hydroxyquinolin-2-yl)cyclohex-3-enecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC=C(c2nc3ccc(OC)cc3cc2Cl)CC1
Reaction #84088
ethyl 4-(3-chloro-6-methoxyquinolin-2-yl)cyclohex-3-enecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cncc(C2=CCCCC2)c1
Reaction #156248
5-cyclohexenylnicotinaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnccc1C1=CCCCC1
Reaction #157056
4-cyclohexenyl-3-nitropyridine
收率 82.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=C(c2ccncc2[N+](=O)[O-])CCC1
Reaction #160750
3-(3-nitropyridin-4-yl)cyclohex-2-enone
收率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(=O)C=C(c2ccncc2[N+](=O)[O-])C1
Reaction #160757
5-methyl-3-(3-nitropyridin-4-yl)cyclohex-2-enone
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=C(c2nccnc2F)CCC1
Reaction #176985
DOI: 10.1039/C8SC04228D
CC1(C)CC=C(c2cc(Br)ccc2N)CC1
Reaction #181577
DOI: 10.1039/C8SC04228D
CC(C)c1cc(C#N)cc2nc(-c3ccc(C(=O)NCC4CC=C(Cc5ccc(C(F)(F)F)cc5)CC4)cc3)oc12
Reaction #185998
DOI: 10.1039/C8SC04228D
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