بحث البنية الفرعية

1377215

O=C(O)c1ccc(-c2ccc3cc(O)ccc3n2)cc1F
Reaction #84065
2-fluoro-4-(6-hydroxyquinolin-2-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Nc1n[nH]c2cc(-c3ccc(C(=O)O)c(F)c3)nc(-c3ccc(Oc4ccccc4)cc3)c12
Reaction #168256
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(C(=O)OCc3ccccc3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)c(F)c6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172872
title compound
المردود 89.2%DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)COc2ccc(C(O)(C(C)c3ccc(-c4ccc(C(=O)OC)c(F)c4)cc3Cl)C(F)(F)F)cc21
Reaction #190649
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(C(=CC2CCCC2)c2cc3cc(C)cnc3n2S(=O)(=O)c2ccccc2)cc1F
Reaction #228100
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(C(=CC2CCOCC2)c2cc3cc(F)cnc3n2S(=O)(=O)c2ccccc2)cc1F
Reaction #240426
DOI: 10.1039/C8SC04228D
CCn1cc(C(O)(C(C)c2ccc(-c3ccc(C(=O)OC)c(F)c3)cc2Cl)C(F)(F)F)ccc1=O
Reaction #245015
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(C(=CC2CCCC2)c2cc3cc(F)cnc3n2S(=O)(=O)c2ccccc2)cc1F
Reaction #388112
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(-c2ccc(C(C)C(O)(c3ccc4c(c3)oc(=O)n4C)C(F)(F)F)c(Cl)c2)cc1F
Reaction #401753
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)c1ccc(-c2ccc(C(=O)O)c(F)c2)cn1
Reaction #402717
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(-c2ccn3c(C(=O)Nc4cc(C(=O)NCc5ccc(F)c(F)c5)ccc4F)cnc3c2)cc1F
Reaction #422470
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CCC[C@H](C)N1CCNC(=O)c1ccc(F)c(NC(=O)c2cnc3cc(-c4ccc(C(=O)O)c(F)c4)ccn23)c1
Reaction #422480
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-c2ccn3c(C(=O)Nc4cc(C(=O)NCc5ccccc5N5CCN(C)CC5)ccc4F)cnc3c2)cc1F
Reaction #422482
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #494050
solid
المردود 19.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(-c2ccc(C(=O)O)c(F)c2F)cn1
Reaction #587448
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(F)c(B(O)O)cc(F)c1C(=O)O
Reaction #595372
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-c2c(C)c(Cl)cc(C(C)=O)c2OC)cc1F
Reaction #598061
Methyl 3′-acetyl-5′-chloro-3-fluoro-2′-methoxy-6′-methylbiphenyl-4-carboxylat
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cccc(CNC(=O)c2ccc(B(O)O)cc2F)c1
Reaction #682973
3-fluoro-4-(3-(methylsulfonyl)benzylcarbamoyl)-phenylboronic acid
المردود 88.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(c1ccccc1)C(F)(F)F)c1ccc(B(O)O)cc1F
Reaction #682974
crude product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN(S(=O)(=O)c2ccccc2F)C1)c1ccc(B(O)O)cc1F
Reaction #682977
(R)-3-fluoro-4-(1-(2-fluorophenylsulfonyl)piperidin-3-ylcarbamoyl)phenylboronic acid
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي