部分構造検索

Cc1ccc(Cl)cc1

O=C(O)c1n[nH]cc1-c1ccc(Cl)cc1Cl
Reaction #48592
4-(2,4-dichloro-phenyl)-1H-pyrazole-3-carboxylic acid
収率 108.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCc2c(Cl)c(Cl)cc(I)c21
Reaction #49515
4,5-dichloro-7-iodoisoindolinone
収率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(Cl)cc1OC(C)C(=O)OC
Reaction #50475
desired material
収率 102.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1Oc2cc(Cl)ccc2C1=O
Reaction #50476
desired product
収率 44.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(c2ccc(Cl)cc2)CCC1
Reaction #57053
Methyl 1-(4-chlorophenyl)cyclobutanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CO)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78924
amide
収率 43.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)ccc(CNC(=O)C(C)(C)C)c1F
Reaction #87617
product
収率 63.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(CCCCl)(C(=O)O)c1ccc(Cl)cc1
Reaction #158273
title compound
収率 83.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)NNC(=O)C(C)(CCCCl)c2ccc(Cl)cc2)ccc1-c1cnc(C)o1
Reaction #158274
title compound
収率 82.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCC(Cc1ccc(Cl)cc1)C(=O)O
Reaction #166741
4-(tert-butoxycarbonylamino)-2-(4-chlorobenzyl)butanoic acid
収率 9.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c[nH]c2ncc(-c3ccccc3)c(N3CCN(C(=O)C(CCNC(=O)OC(C)(C)C)Cc4ccc(Cl)cc4)CC3)c12
Reaction #166742
tert-butyl 3-(4-chlorobenzyl)-4-(4-(3-methyl-5-phenyl-1H-pyrrolo[2,3-b]pyri din-4-yl)piperazin-1-yl)-4-oxobutylcarbamate
収率 12.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(Cc1ccc(Cl)cc1)C(=O)N1CCN(c2c(Br)cnc3[nH]ncc23)CC1
Reaction #176714
DOI: 10.1039/C8SC04228D
CC(=O)N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)C1CCCN(C(=O)OC(C)C)c2cc(Cl)c(C)cc21
Reaction #177688
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(N(CC(N)=O)Cc2ccc(Cl)cc2)C1
Reaction #180339
DOI: 10.1039/C8SC04228D
Cc1nn(C)c(OCCN(C)c2ccccc2)c1C(=O)c1ccc(Cl)cc1Cl
Reaction #182073
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(Cc1ccc(Cl)cc1)C(=O)N1CCC(CO)(N2CCCCC2)CC1
Reaction #183565
DOI: 10.1039/C8SC04228D
OCc1cn(Cc2ccc(Cl)c(Cl)c2)nn1
Reaction #185938
DOI: 10.1039/C8SC04228D
C=CCn1nc(C)c(C(=O)c2ccc(Cl)cc2Cl)c1OS(=O)(=O)c1ccc(C)cc1
Reaction #191547
DOI: 10.1039/C8SC04228D
CN(Cc1ccc(Cl)c(Cl)c1)C(=O)C1=C(O)C(=O)N(CCN2CCCCC2)C1
Reaction #192085
DOI: 10.1039/C8SC04228D
Cc1ccc(C(=O)COc2c(C(=O)c3ccc(Cl)cc3Cl)c(C)nn2C)cc1
Reaction #194272
DOI: 10.1039/C8SC04228D
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