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Cc1cccc(CCl)n1

FC(F)(F)c1cccc(CCl)n1
Reaction #45292
2-chloromethyl-6-trifluoromethylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
COCCCc1nc(C(F)F)ccc1C(=O)OC
Reaction #48275
6-Difluoromethyl-2-(3-methoxy-propyl)-nicotinic acid methyl ester
Выход 113.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cccc(CCl)n2)cc1
Reaction #50536
2-(4- methylphenyl)-6-chloromethylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(-c2cccc(COc3ccc(CCCCn4ccnn4)cc3)n2)cc1
Reaction #61784
title compound
Выход 60.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCc2cccc(-c3ccc(C(F)(F)F)cc3)n2)ccc1CCCCn1ccnn1
Reaction #61785
title compound
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCc2cccc(-c3ccc(OC(F)(F)F)cc3)n2)ccc1CCCCn1ccnn1
Reaction #61796
title compound
Выход 79.2%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)Oc1ccc(-c2cccc(COc3ccc(CCCCn4ccnn4)cc3)n2)cc1
Reaction #61797
title compound
Выход 18.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCc2cccc(-c3ccc(Cl)cc3)n2)ccc1CCCCn1ccnn1
Reaction #61803
title compound
Выход 78.6%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(-c2cccc(COc3ccc(CCCCn4ccnn4)cc3)n2)cc1
Reaction #61804
title compound
Выход 47.0%DOI: 10.6084/m9.figshare.5104873.v1
ClCc1cccc(-c2cccc(Cl)c2)n1
Reaction #61816
2-Chloromethyl-6-(3-chloro-phenyl)-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCc2cccc(-c3cccc(Cl)c3)n2)ccc1CCCCn1ccnn1
Reaction #61817
title compound
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(NCc1ccncc1)c1cccc(C(=O)N2Cc3ccccc3Oc3ccc(Cl)cc32)n1
Reaction #65634
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1cccc(-c2ccccc2)n1
Reaction #74196
6-Phenyl-pyridine-2-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H](CC(=O)c1cccc(-c2ccccc2)n1)C(=O)O
Reaction #74197
title compound
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(COc2ccc(Cc3cc(-c4cccnc4N)on3)cc2)n1
Reaction #165001
title compound
Выход 51.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(CCl)n1
Reaction #165002
title compound
Выход 85.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(Cn2nc(Br)c3c([N+](=O)[O-])cccc32)n1
Reaction #166425
desired product
Выход 80.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(Cn2nc(Br)c3c([N+](=O)[O-])cccc32)n1
Reaction #166582
3-bromo-1-((6-methylpyridin-2-yl)methyl)-4-nitro-1H-indazole
Выход 80.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC(O)(c1ccc(Cl)cc1)c1ccc(OCc2cccc(C)n2)cc1
Reaction #173360
DOI: 10.1039/C8SC04228D
COc1ccc(C2=C(c3ccc(OCc4cccc(C)n4)cc3)COC2=O)cc1
Reaction #177531
DOI: 10.1039/C8SC04228D
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