子结构搜索

61409

COC(=O)c1cc(O)c2c3c(cc(Br)c2n1)S(=O)(=O)c1ccccc1-3
Reaction #415898
methyl 5-bromo-1-hydroxy[1]-benzothieno[3,2-f]quinoline-3-carboxylate-7,7-dioxide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(-c3ccccc3)cccc2n1
Reaction #833440
5-Phenylquinaldine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(-c3ccc(Cl)cc3)c(O)c(Cl)cc2n1
Reaction #1018882
1E
收率 47.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1c(Cl)cc2nc(C)ccc2c1-c1ccc(Cl)cc1
Reaction #1018883
desired product 1G
收率 35.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(-c3ccc(Cl)cc3)c([C@H](O)CO)c(Cl)cc2n1
Reaction #1018884
desired product 1H
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(-c3ccc(Cl)cc3)c([C@@H](COC(=O)C(C)(C)C)OC(C)(C)C)c(Cl)cc2n1
Reaction #1018885
desired product 1J
收率 155.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(-c3ccc(Cl)cc3)c([C@@H](CO)OC(C)(C)C)c(Cl)cc2n1
Reaction #1018886
desired product 1K
收率 61.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(-c3ccc(Cl)cc3)c([C@H](OC(C)(C)C)C(=O)O)c(C)cc2n1
Reaction #1018887
(S)-2-tert-butoxy-2-(5-(4-chlorophenyl)-2,7-dimethylquinolin-6-yl)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(-c3ccc(Cl)cc3)c(O)c(C)cc2n1
Reaction #1018890
Compound 2D
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(-c3ccc(Cl)cc3)c(OS(=O)(=O)C(F)(F)F)c(C)cc2n1
Reaction #1018891
Compound 2E
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1c(C)cc2nc(C)ccc2c1-c1ccc(Cl)cc1
Reaction #1018892
Compound 2F
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(-c3ccc(Cl)cc3)c([C@H](O)CO)c(C)cc2n1
Reaction #1018893
Compound 2G
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(-c3ccc(Cl)cc3)c([C@@H](COC(=O)C(C)(C)C)OC(C)(C)C)c(C)cc2n1
Reaction #1018894
Compound 2I
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2ncccc2c(-c2ccc(Cl)cc2)c1[C@H](OC(C)(C)C)C(=O)O
Reaction #1018895
(S)-2-tert-butoxy-2-(5-(4-chlorophenyl)-7-methylquinolin-6-yl)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2ncccc2c(-c2ccc(Cl)cc2)c1O
Reaction #1018899
Compound 3E
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2ncccc2c(-c2ccc(Cl)cc2)c1OS(=O)(=O)C(F)(F)F
Reaction #1018900
Compound 3F
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1c(C)cc2ncccc2c1-c1ccc(Cl)cc1
Reaction #1018901
Compound 3G
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2ncccc2c(-c2ccc(Cl)cc2)c1[C@H](O)CO
Reaction #1018902
Compound 3H
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2ncccc2c(-c2ccc(Cl)cc2)c1[C@@H](COC(=O)C(C)(C)C)OC(C)(C)C
Reaction #1018903
Compound 3J
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2ncccc2c(-c2ccc(Cl)cc2)c1[C@@H](CO)OC(C)(C)C
Reaction #1018904
Compound 3K
DOI: 10.6084/m9.figshare.5104873.v1
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