Поиск подструктуры

15628

CC(C)OC(=O)Cn1c(=O)n(C)c(=O)n(-c2cc(N3C(=O)C4CS(=O)CCN4C3=O)c(F)cc2Cl)c1=O
Reaction #1570
title product
Выход 60.4%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCN1C(=O)c2cccc3cc4cccc(NC(=O)Cc5ccc(Cl)cc5)c4c(c23)C1=O
Reaction #46407
desired product
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Nc1cccc2cc3cccc4c3c(c12)C(=O)N(CCN(C)C)C4=O
Reaction #46411
desired product
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCOC(=O)Nc1cccc2cc3cccc4c3c(c12)C(=O)N(CCN(C)C)C4=O
Reaction #46417
desired product
Выход 93.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)Nc1cccc2cc3cccc4c3c(c12)C(=O)N(CCN(C)C)C4=O
Reaction #46418
desired product
Выход 51.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #46420
powder
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #46421
powder
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)Cn1c(=O)n(C)c(=O)n(-c2cc(N3C(=O)C4CS(=O)CCN4C3=O)c(F)cc2Cl)c1=O
Reaction #80697
title product
Выход 60.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCc1c[nH]c2ccc(Cl)cc12)C1CCN(c2cccc(-n3cccc3)c2)C1=O
Reaction #86993
1-(3-(1H-pyrrol-1-yl)phenyl)-N-(2-(5-chloro-1H-indol-3-yl)ethyl)-2-oxopyrrolidine-3-carboxamide
Выход 30.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCc1c[nH]c2ccc(Cl)cc12)C1CCN(c2ccc(C(F)(F)F)cc2)C1=O
Reaction #86998
N-(2-(5-chloro-1H-indol-3-yl)ethyl)-2-oxo-1-(4-(trifluoromethyl)phenyl)pyrrolidine-3-carboxamide
Выход 7.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCc1c[nH]c2ccc(Cl)cc12)C1CCN(c2ccc(C(F)(F)F)c(F)c2)C1=O
Reaction #87000
N-(2-(5-chloro-1H-indol-3-yl)ethyl)-1-(3-fluoro-4-(trifluoromethyl)phenyl)-2-oxopyrrolidine-3-carboxamide
Выход 20.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N2C(=O)C3C(O)CCN3C2=O)c2cccnc12
Reaction #188331
DOI: 10.1039/C8SC04228D
CCC1c2cc(F)ccc2-c2ccccc2N1C(=O)c1ccc(O)cc1
Reaction #195115
DOI: 10.1039/C8SC04228D
Cc1noc(C)c1S(=O)(=O)N1CCC2(CCN(c3ccc(OC(F)(F)F)cc3)C2=O)CC1
Reaction #195326
DOI: 10.1039/C8SC04228D
CC(=O)N(CC(=O)NC(C)C(=O)N1C(=O)C(C)c2ccccc2-c2c(N)cccc21)c1ccccc1
Reaction #197177
DOI: 10.1039/C8SC04228D
CN(C)c1cc2c(cc1C(F)(F)F)NC(=O)CC(c1cccc(-c3cc(CN4CCCC4)no3)c1)=N2
Reaction #206354
DOI: 10.1039/C8SC04228D
CS(=O)(=O)OC1CN2C(=O)N(c3cc(Cl)cc(Cl)c3)C(=O)C2(Cc2ccc(Br)cc2)C1
Reaction #226954
DOI: 10.1039/C8SC04228D
CC1(C)CCn2c1cc1cc(NC(=O)C3(c4ccc5c(c4)OCO5)CC3)ccc12
Reaction #232836
DOI: 10.1039/C8SC04228D
Cc1noc(C)c1S(=O)(=O)N1CCC2(CCN(c3ccc(C(F)(F)F)cc3)C2=O)CC1
Reaction #247158
DOI: 10.1039/C8SC04228D
CC(C)c1[nH]n(-c2c(Cl)cc(Cl)cc2Cl)c2nc(Cc3ccc(NC(=O)CCl)cc3)nc(=O)c1-2
Reaction #247303
DOI: 10.1039/C8SC04228D
Страница 1Далее