Поиск подструктуры

ClCc1ccc(Cl)nc1

Clc1ccc(COc2ccc(Oc3ccccc3)cc2Cl)cn1
Reaction #5300
2-chloro-5-(2-chloro-4-phenoxyphenoxy)methylpyridine
Выход 70.8%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cccc(Oc2ccc(OCc3ccc(Cl)nc3)c(Cl)c2)c1
Reaction #5301
2-chloro-5-[2-chloro-4-(3-trifluoromethylphenoxy)phenoxy]methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(COc2ccc(Oc3cccc(Br)c3)cc2Cl)cn1
Reaction #5302
2-chloro-5-[4-(3-bromophenoxy)-2-chlorophenoxy]methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCCn1c(=O)c2[nH]c(-c3ccc(Cl)nc3)nc2n(CCC)c1=O
Reaction #42898
solid
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])C=C1SCCN1Cc1ccc(Cl)nc1
Reaction #50485
3-(2-chloro-5-pyridylmethyl)-2-nitromethylenethiazolidine
Выход 29.8%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])N=C1SCCN1Cc1ccc(Cl)nc1
Reaction #50494
3-(2-chloro-5-pyridylmethyl)-2-(nitroimino)thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(Cl)c1ccc(Cl)nc1
Reaction #70835
desired product
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)COC(=O)c1ccc(Cl)nc1
Reaction #73527
2,2-dimethylpropyl 6-chloropyridine-3-carboxylate
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(CCl)c(Cl)nc1Cl
Reaction #76157
2,6-dichloro-5-fluoronicotinyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #93804
1a
DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc2cc(OCc3ccc(Cl)nc3)ccc2[nH]1
Reaction #164623
6-((6-chloropyridin-3-yl)methoxy)quinolin-2(1H)-one
Выход 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(Cc2ccc(Cl)nc2)CC1
Reaction #166383
compound 339
Выход 84.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1CCN(Cc2ccc(Cl)nc2)CC1
Reaction #166388
compound 348
Выход 30.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(C(=O)c2cccnc2Cl)CC1
Reaction #166391
compound 351
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CN(Cc2ccc(Cl)nc2)CCN1
Reaction #166393
compound 356
Выход 34.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(Cc2ccc(Cl)nc2)C(=O)C1
Reaction #166395
compound 358
Выход 93.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC(O)CN1CCC(Oc2ccc(Cl)c(Cl)c2)CC1)c1cnc(Cl)cc1C(F)(F)F
Reaction #173054
DOI: 10.1039/C8SC04228D
Fc1cc(CCl)c(Cl)nc1Cl
Reaction #173264
DOI: 10.1039/C8SC04228D
[O-][n+]1cc(CN2CCOCC2)ccc1Cl
Reaction #173652
DOI: 10.1039/C8SC04228D
[O-][n+]1cc(CN2CCN(c3ccccc3)CC2)ccc1Cl
Reaction #175107
DOI: 10.1039/C8SC04228D
Страница 1Далее