بحث البنية الفرعية

1319197

COc1cc(C(=O)N2CCOC(CCO)(c3ccc(Cl)c(Cl)c3)C2)cc(OC)c1OC
Reaction #174661
DOI: 10.1039/C8SC04228D
Cc1ccc(S(=O)(=O)OCCC2(c3ccc(Cl)c(Cl)c3)CN(C(=O)Cc3cc(C(F)(F)F)cc(C(F)(F)F)c3)CCO2)cc1
Reaction #198209
DOI: 10.1039/C8SC04228D
COc1cc(C(=O)N2CCO[C@](CCOS(=O)(=O)c3ccc(Cl)cc3)(c3ccc(Cl)c(Cl)c3)C2)cc(OC)c1OC
Reaction #314725
title compound
المردود 95.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)N2CCOC(CCOS(=O)(=O)c3ccc(Cl)cc3)(c3ccc(Cl)c(Cl)c3)C2)cc(OC)c1OC
Reaction #314726
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)N2CCO[C@](CCO)(c3ccc(Cl)c(Cl)c3)C2)cc(OC)c1OC
Reaction #314727
(2R)-2-[2-(3,4-dichlorophenyl)-4-(3,4,5-trimethoxybenzoyl)morpholin-2-yl]ethanol
المردود 104.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)N2CCOC(CCOS(=O)(=O)c3ccc([N+](=O)[O-])cc3)(c3ccc(Cl)c(Cl)c3)C2)cc(OC)c1OC
Reaction #314728
title compound
المردود 94.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OCC[C@@]2(c3ccc(Cl)c(Cl)c3)CN(C(=O)Cc3cc(C(F)(F)F)cc(C(F)(F)F)c3)CCO2)cc1
Reaction #314729
title compound
المردود 60.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OCCC2(c3ccc(Cl)c(Cl)c3)CN(C(=O)Cc3cc(C(F)(F)F)cc(C(F)(F)F)c3)CCO2)cc1
Reaction #314730
title compound
المردود 63.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)N1CCOC(CCOS(=O)(=O)c2ccc(Cl)cc2)(c2ccc(Cl)c(Cl)c2)C1
Reaction #314731
title compound
المردود 47.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)N1CCO[C@](CCO)(c2ccc(Cl)c(Cl)c2)C1
Reaction #314734
title compound
المردود 68.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)N1CCOC(CCO)(c2ccc(Cl)c(Cl)c2)C1
Reaction #314735
title compound
المردود 58.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O.O=C1COC(CCN2CCC(C(=O)N3CCCC3)(c3ccccc3)CC2)(c2ccc(Cl)c(Cl)c2)CN1Cc1ccccc1
Reaction #449908
expected product
المردود 58.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N(C)C1(c2ccccc2)CCN(CCC2(c3ccc(Cl)c(Cl)c3)CN(Cc3ccccc3)C(=O)CO2)CC1.Cl.O
Reaction #449909
expected product
المردود 79.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)NC1(c2ccccc2)CCN(CCC2(c3ccc(Cl)c(Cl)c3)CN(Cc3ccccc3)C(=O)CO2)CC1.Cl.O
Reaction #449910
expected product
المردود 65.2%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O.O=C1COC(CCN2CCC(NC(=O)N3CCCC3)(c3ccccc3)CC2)(c2ccc(Cl)c(Cl)c2)CN1Cc1ccccc1
Reaction #449914
expected product
المردود 65.2%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1nc(C2(c3ccccc3)CCN(CCC3(c4ccc(Cl)c(Cl)c4)CN(Cc4ccccc4)C(=O)CO3)CC2)cs1.Cl.Cl
Reaction #449915
expected product
المردود 131.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O.O.O=C(c1ccccc1)N1CCOC(CCN2CCC(C(=O)NN3CCCC3)(c3ccccc3)CC2)(c2ccc(Cl)c(Cl)c2)C1
Reaction #449916
expected product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)N2CCOC(CCO)(c3ccc(Cl)c(Cl)c3)C2)cc(OC)c1OC
Reaction #786400
DOI: 10.1039/C8SC04228D
CC(C)Oc1cccc(CC(=O)N2CCOC(CCO)(c3ccc(Cl)c(Cl)c3)C2)c1
Reaction #894171
DOI: 10.1039/C8SC04228D
O=C(c1cc(C(F)(F)F)cc(C(F)(F)F)c1)N1CCOC(CCO)(c2ccc(Cl)c(Cl)c2)C1
Reaction #902351
DOI: 10.1039/C8SC04228D
الصفحة 1التالي