بحث البنية الفرعية

1349698

O=C(Nc1ccccc1-c1ccccc1)OC1CCN(CCNCCc2ccccc2)CC1
Reaction #42133
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(C(=O)NCCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)cc1
Reaction #42134
title intermediate
المردود 92.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCN1CCC(OC(=O)Nc2ccccc2-c2ccccc2)CC1
Reaction #42135
title intermediate
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCN1CCC(OC(=O)Nc2ccccc2-c2ccccc2)CC1)NCc1cccc(CO)c1
Reaction #42136
title intermediate
المردود 57.3%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cccc(CNC(=O)CCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)c1
Reaction #42137
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NCc1ccc(NC(=O)CCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)cc1
Reaction #42138
title intermediate
المردود 94.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(NC(=O)CCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)cc1
Reaction #42139
title intermediate
المردود 66.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C(=O)N(C)CCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)c(OC)c1
Reaction #42142
title intermediate
المردود 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C=O)ccc1C(=O)CNCCN1CCC(OC(=O)Nc2ccccc2-c2ccccc2)CC1
Reaction #42143
Biphenyl-2-ylcarbamic acid 1-{2-[(4-formyl-2-methoxybenzoyl)methylamino]ethyl}piperidin-4-yl Ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1-c1ccccc1)OC1CCN(CCNCC(=O)c2cccc(C(=O)NCCNCc3ccc(O)cc3)c2)CC1
Reaction #175025
DOI: 10.1039/C8SC04228D
O=C(CCN1CCC(OC(=O)Nc2ccccc2-c2ccccc2)CC1)NCc1cccc(CO)c1
Reaction #176201
DOI: 10.1039/C8SC04228D
O=Cc1cccc(CNC(=O)CCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)c1
Reaction #176997
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
CN(CCN1CCC(OC(=O)Nc2ccccc2-c2ccccc2)CC1)C(=O)CCCCCN(C(=O)OCc1ccccc1)c1ccc(N(C)C(=O)OC(C)(C)C)cc1
Reaction #190866
DOI: 10.1039/C8SC04228D
CNCCCN(OC)C(=O)c1ccc(NCCCCCC(=O)N(C)CCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)cc1
Reaction #190875
DOI: 10.1039/C8SC04228D
CN(CCN1CCC(OC(=O)Nc2ccccc2-c2ccccc2)CC1)C(=O)CCCCCNc1ccc2c(c1)CCN(CCCN(C)C(=O)OC(C)(C)C)C2
Reaction #195851
DOI: 10.1039/C8SC04228D
COC(=O)CCCNCC(=O)CCN1CCC(OC(=O)Nc2ccccc2-c2ccccc2)CC1
Reaction #196138
DOI: 10.1039/C8SC04228D
Cc1cc(NC(=O)CCCCN(C)C(=O)CCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)c(C)cc1CNCC(O[Si](C)(C)C(C)(C)C)c1ccc(O)c2[nH]c(=O)ccc12
Reaction #196594
DOI: 10.1039/C8SC04228D
CN(CCN1CCC(OC(=O)Nc2ccccc2-c2ccccc2)CC1)C(=O)CCCCCNc1ncc(Br)cn1
Reaction #202672
DOI: 10.1039/C8SC04228D
Cc1cc(NC(=O)CCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)c(C)cc1C=NCC(O[Si](C)(C)C(C)(C)C)c1ccc(O)c(NC=O)c1
Reaction #211700
DOI: 10.1039/C8SC04228D
الصفحة 1التالي