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13605

COC(=O)c1cc(Nc2ccccc2)cc(B2OC(C)(C)C(C)(C)O2)c1
Reaction #597
Выход 2.3%
COC(=O)c1cc(Nc2ccccc2)cc(B2OC(C)(C)C(C)(C)O2)c1
Reaction #598
Выход 0.0%
O=Cc1cccc(-c2cc3[nH]c4ccc(O)cc4c3c3c2C(=O)NC3=O)c1
Reaction #11127
3-(9-Hydroxy-1,3-dioxo-1,2,3,6-tetrahydropyrrolo[3,4-c]carbazol-4-yl)benzaldehyde
Выход 69.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cccc(-c2ccnc(Cl)n2)c1
Reaction #42979
3-(2-Chloro-pyrimidin-4-yl)-benzaldehyde
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cccc(-c2ccnc(Cl)n2)c1
Reaction #43081
1-[3-(2-Chloro-pyrimidin-4-yl)-phenyl]-ethanone
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cccc(-c2ccnc(NCCc3ccc(O)cc3)n2)c1
Reaction #43113
1-(3-{2-[2-(4-Hydroxy-phenyl)-ethylamino]-pyrimidin-4-yl}-phenyl)-ethanone
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C=O)cc1-c1ccnc(Cl)n1
Reaction #43251
3-(2-chloropyrimidin-4-yl)4-methylbenzaldehyde
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cccc(-c2ccnc(Cl)n2)c1
Reaction #43261
3-(2-Chloro-pyrimidin-4-yl)-benzaldehyde
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cccc(-c2ccc3c(c2)CC(NS(=O)(=O)C(C)C)C3)c1
Reaction #46701
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cccc(-c2ccc(COc3ccc(C(=O)O)c(O)c3)cc2)c1
Reaction #46715
4-(3′-Acetyl-biphenyl-4-ylmethoxy)-2-hydroxy-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)O)cc1-c1cc(C=O)c(C(=O)NC(C)(C)C)s1
Reaction #47858
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cccc(-c2cc3c(Br)ccnc3n2S(=O)(=O)c2ccccc2)c1
Reaction #57233
title compound
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(B2OC(C)(C)C(C)(C)O2)cc(C)c1OC(=O)c1oc2ccccc2c1C
Reaction #57730
3-methyl-benzofuran-2-carboxylic acid 2,6-dimethyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl ester
Выход 28.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)O)ccc1-c1cc(C)c(OCCN[C@@H](C)[C@H](O)c2ccc(O)cc2)c(C)c1
Reaction #59048
title compound
Выход 22.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(NC(=O)c2ccc(C)c(B3OC(C)(C)C(C)(C)O3)c2)c1
Reaction #59681
solid
Выход 73.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)Nc2nccs2)cc1B1OC(C)(C)C(C)(C)O1
Reaction #59692
4-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-N-(thiazol-2-yl)-benzamide
Выход 65.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)Nc2nncs2)cc1B1OC(C)(C)C(C)(C)O1
Reaction #59693
4-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-N-([1,3,4]thiadiazol-2-yl)-benzamide
Выход 36.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)NCC2CC2)cc1B1OC(C)(C)C(C)(C)O1
Reaction #59696
N-cyclopropylmethyl-4-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzamide
Выход 71.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)Nc2cccc(N3CCOCC3)c2)cc1-c1ccc(-c2csc(N)n2)cc1
Reaction #59709
4′-(2-Amino-4-thiazolyl)-6-methyl-N-[3-(4-morpholinyl)phenyl][1,1′-biphenyl]-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc(-c2ccc(-c3cc(C(=O)Nc4cccc(N5CCOCC5)c4)ccc3C)c(C)c2)o1
Reaction #59710
2′,6-Dimethyl-4′-(5-methyl-1,3,4-oxadiazol-2-yl)-N-[3-(4-morpholinyl)phenyl][1,1′-biphenyl]-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
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