部分構造検索

378201

O=C([O-])C(F)(F)F
Reaction #48762
trifluoroacetate
収率 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@]1(O)C[C@H]2CN(CCc3c([nH]c4c(I)cccc34)[C@@](C(=O)OC)(c3cc4c(cc3OC)N(C)[C@H]3[C@@](O)(C(=O)OC)[C@H](OC(C)=O)[C@]5(CC)C=CCN6CC[C@]43[C@@H]65)C2)C1
Reaction #48763
12′-iodovinblastine
収率 112.4%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CC1(C(=O)O)CC1
Reaction #62402
mixture
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1(CO)CCCC1
Reaction #69291
product
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1(C=O)CCCC1
Reaction #69292
product
収率 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1(CO)CCCC1
Reaction #73323
product
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1(C=O)CCCC1
Reaction #73324
product
収率 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(C(=O)Nc2cnn3ccc(N4CCC[C@@H]4c4cc(F)ccc4F)nc23)CC1
Reaction #92287
final product
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1(C(=O)Nc2cnn3ccc(N4CCC[C@@H]4c4cc(F)ccc4F)nc23)CC1
Reaction #92288
final product
収率 82.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C(=O)O)CCCNC1
Reaction #157088
3-methylpiperidine-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C(=O)O)CCCN(c2ccncc2[N+](=O)[O-])C1
Reaction #157089
3-methyl-(3-nitropyridin-4-yl)piperidine-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CCN(c2nc(-c3c(C)ccc4[nH]nc(C)c34)nc3c2CN(c2c(Cl)c(C4CC4)nn2C)CC3)CC1(C)C
Reaction #168024
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CCN(c2nc(-c3c(C)ccc4[nH]nc(C)c34)nc3c2CN(c2c(C#N)c(C(F)F)nn2C)CC3)CC1(C)C
Reaction #168047
(R)-3-(difluoromethyl)-5-(2-(3,5-dimethyl-1H-indazol-4-yl)-4-(4-methoxy-3,3-dimethylpiperidin-1-yl)-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)-1-methyl-1H-pyrazole-4-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CO)CNC(=O)c1ccc(OCc2conc2-c2ccc(Cl)cc2)nc1
Reaction #170628
title compound
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1(C(=O)Nc2cnn3ccc(N4CCCC4c4cc(F)ccc4F)nc23)CC1
Reaction #174526
DOI: 10.1039/C8SC04228D
COC(=O)C1(C(=O)Nc2cnn3ccc(N4CCCC4c4cc(F)ccc4F)nc23)CC1
Reaction #181417
DOI: 10.1039/C8SC04228D
CC1(C)COc2cccnc2NC1=O
Reaction #181609
DOI: 10.1039/C8SC04228D
O=C1C2CC2(C(=O)O)C(=O)N1c1ccc(-n2ccccc2=O)cc1F
Reaction #183942
DOI: 10.1039/C8SC04228D
COCC12Cc3cnn(-c4ccc(F)cc4)c3C=C1CCN(S(=O)(=O)c1ccc(N3CCC(F)C3)nc1)C2
Reaction #195531
DOI: 10.1039/C8SC04228D
O=C(O)C1(C(=O)Nc2ccc(-c3ccccc3)cc2)CC1
Reaction #201590
DOI: 10.1039/C8SC04228D
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