Busqueda de Subestructura

CCCCCCN(C)C

O=C(OCC12CCCN(CCC1)C2)c1c[nH]c2ccccc12
Reaction #5482
colorless crystals
Rendimiento 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(C#N)(CCCN(C)CCCOc2ccccc2N)C(C)C)cc(OC)c1OC
Reaction #93375
desired compound
Rendimiento 105.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(CC(O)c2cc(-c3ccccc3)nc3ccccc23)CC1
Reaction #93498
2-(1-methyl-4-piperidyl)-1-(2-phenyl-4-quinolyl)-ethanol
Rendimiento 37.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCc1ccc(CC2SCC(=O)N2CCC2(O)CCCCC2)cc1
Reaction #175271
DOI: 10.1039/C8SC04228D
CC(C)CC=C1CCC2(CC1)SCC(=O)N2CCC(=O)O
Reaction #175927
DOI: 10.1039/C8SC04228D
CC(C)C(=O)Nc1cccc(C2CCN(CCCCCC(Oc3ccc(Br)cc3)c3ccc(Cl)cc3)CC2)c1
Reaction #177485
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCCCCC(NC(=O)C(N)Cc1cc(Cl)c(O)c(Cl)c1)C(=O)N1CCN(c2ccncc2)CC1
Reaction #177823
DOI: 10.1039/C8SC04228D
CC(C)C(=O)Nc1cccc(C2CCN(CCCCCC(Oc3cc(C(F)(F)F)ccc3F)c3ccc(F)cc3)CC2)c1
Reaction #178764
DOI: 10.1039/C8SC04228D
CN(CCN1CCC(OC(=O)Nc2ccccc2-c2ccccc2)CC1)C(=O)CCCCCNc1ccc(CC(=O)N(C)CCCN(C)C(=O)COC2Cc3ccccc3C23CCN(CCC2(c4ccc(F)cc4)CN(C(=O)c4cc(C(F)(F)F)cc(C(F)(F)F)c4)CO2)CC3)cc1
Reaction #187623
DOI: 10.1039/C8SC04228D
CC(=O)Oc1ccc(C2C(CCC(OC(C)=O)c3ccc(F)cc3)C(=O)N2c2ccc(C#CCNS(C)(=O)=O)cc2)cc1
Reaction #188100
DOI: 10.1039/C8SC04228D
O=C(O)C1CC(C2CCCCC2)CN1C(=O)CP(=O)(O)CCCCc1ccccc1
Reaction #190894
DOI: 10.1039/C8SC04228D
CCCCCCN(Cc1ccc(C#Cc2ccc(CCCC)cc2)cc1)c1ccc(F)c(C(=O)OC)c1
Reaction #192930
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCC(CCN2CCC(C(=O)c3cc(Cl)ccc3Cl)CC2)CC1
Reaction #193113
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCc1cc(Cl)c(NC(=O)CN2CCN(CCCCC(c3ccc(F)cc3)c3ccc(F)cc3)CC2C(N)=O)c(Cl)c1
Reaction #196096
DOI: 10.1039/C8SC04228D
COc1cc(C(=O)N(C)c2ccc(C)cc2OCCCCCC(=O)N2CCC(N(C)C)CC2)ccc1NC(=O)c1ccccc1O
Reaction #200686
DOI: 10.1039/C8SC04228D
CN(CCN1CCC(OC(=O)Nc2ccccc2-c2ccccc2)CC1)C(=O)CCCCCNc1ncc(Br)cn1
Reaction #202672
DOI: 10.1039/C8SC04228D
COC(=O)NCC1CCC(C(=O)N2CC(c3ccc(F)cc3)C(N(C)C(=O)N(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C2)CC1
Reaction #205365
DOI: 10.1039/C8SC04228D
CN1CCC(CC(O)c2cc(-c3ccccc3)nc3ccccc23)CC1
Reaction #209237
DOI: 10.1039/C8SC04228D
CCCCCCCCCCC[C@H](CC(O)C(C(=O)OC)N(Cc1ccccc1)c1ccccc1)O[Si](C)(C)C(C)(C)C
Reaction #216252
methyl (5R)-2-(N-benzylanilino)-5-(t-butyldimethylsiloxy)-3-hydroxyhexadecanoate
Rendimiento 7.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(Oc2ccc(C(=O)N3CCN(C4CCCCC4O)CC3)cc2)nc1)c1ccc(C(F)(F)F)cc1
Reaction #223034
DOI: 10.1039/C8SC04228D
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