部分構造検索

11256

CC(C)N1C(=O)[C@@H](CC(=O)NCC(=O)O)O[C@@H](c2ccccc2)c2cc(Cl)ccc21
Reaction #1881
N-(cis-7-chloro-1-isopropyl-5-phenyl-1,2,3,5-tetrahydro-2-oxo-4,1-benzoxazepin-3-ylacetyl)glycine
収率 64.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1[C@@H]([C@@H](C)O)C(=O)N1C(Cc1ccc(OC)cc1)Cc1ccc(OC)cc1
Reaction #49991
(3S,4S)-4-methoxycarbonyl-3-(1-(R)-hydroxyethyl)-1-di(p-anisyl)methyl-2-azetidinone
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc2c(ncn2CC2CCCCO2)c(F)c1Nc1ccc(Br)cc1Cl
Reaction #60276
product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NOCCO)c1cc2c(ncn2CC2CCCCO2)c(F)c1Nc1ccc(Br)cc1Cl
Reaction #60277
pure desired product
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc2c(ncn2CCS(C)(=O)=O)c(F)c1Nc1ccc(Br)cc1Cl
Reaction #60280
pure desired product
収率 59.1%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)CCn1cnc2c(F)c(Nc3ccc(Br)cc3Cl)c(CO)cc21
Reaction #60303
clean desired product
収率 79.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc2[nH]c(COCC[Si](C)(C)C)nc2c(F)c1Nc1ccc(C#N)cc1C
Reaction #60321
desired product
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc(C(=O)OC)ccc2Cl)c(=O)n1Cc1ccc(Br)cc1F
Reaction #64562
title compound
収率 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCNC(=O)c1ccc(Cl)c(-n2nc(CCCC)n(Cc3ccc(Br)cc3F)c2=O)c1
Reaction #64563
4-(4-Bromo-2-fluorobenzyl)-5-n-butyl-2-[5-(N-n-butylcarbamoyl)-2-chloro-phenyl]-2,4-dihydro-3H-1,2,4-triazol-3-one
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(NC2=CC(=O)CC(c3ccc(C(F)(F)F)cc3)C2)c1Br
Reaction #79612
3-(3-carbomethoxy-2-bromoanilino)-5-(4-trifluoromethylphenyl)-cyclohex-2-en-1-one
収率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc2[nH]c3c(c12)C(=O)CC(c1ccc(C(F)(F)F)cc1)C3
Reaction #79613
5-carbomethoxy-1,2-dihydro-2-(4-trifluoromethylphenyl)-9H-carbazol-4(3H)-one
収率 87.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CN2C(=O)CC[C@H]2C(=O)O)cc1
Reaction #83395
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)cc1C(=O)O
Reaction #87524
desired product
収率 0.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)ccc1C(=O)O
Reaction #87530
desired product
収率 0.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)cc1C(=O)NCc1ccccc1C(F)(F)F
Reaction #87713
desired product
収率 24.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)cc1C(=O)NC1(c2ccccc2C(F)(F)F)CC1
Reaction #87714
desired product
収率 16.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)cc1C(=O)NC1(c2ccc(C(F)(F)F)cc2)CC1
Reaction #87716
desired product
収率 16.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)ccc1C(=O)NCc1ccccc1C(F)(F)F
Reaction #87718
desired product
収率 17.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)ccc1C(=O)NC1(c2ccccc2C(F)(F)F)CC1
Reaction #87719
desired product
収率 13.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)ccc1C(=O)NC1(c2ccc(C(F)(F)F)cc2)CC1
Reaction #87720
desired product
収率 13.5%DOI: 10.6084/m9.figshare.5104873.v1
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