子结构搜索

230127

COCC(C)(O)c1ccc2c(n1)N1[C@H](C2)CN(C(=O)OC(C)(C)C)C[C@H]1C
Reaction #12050
(4R,9aR)-6-(1-(RS)-Hydroxy-2-methoxy-1-methyl-ethyl)-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C(=O)COc2ccc(CC3SC(=O)NC3=O)cc2)nc1
Reaction #175767
DOI: 10.1039/C8SC04228D
CCc1ccc(C(O)COc2ccc(C=O)cc2)nc1
Reaction #236238
DOI: 10.1039/C8SC04228D
CCc1ccc(C(O)COc2ccc(C=O)cc2)nc1
Reaction #283429
DOI: 10.1039/C8SC04228D
CCc1ccc(C(O)COc2ccc(C=O)cc2)nc1
Reaction #292916
DOI: 10.1039/C8SC04228D
CCc1ccc(C(O)COc2ccc(C=O)cc2)nc1
Reaction #337331
desired product
收率 68.7%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C(O)COc2ccc(C=O)cc2)nc1
Reaction #337332
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C(O)COc2ccc(C=O)cc2)nc1
Reaction #337333
4-[2-(5-ethyl-pyridin-2-yl)-2-hydroxy-ethoxy]-benzaldehyde
收率 68918.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C(O)COc2ccc(C=O)cc2)nc1
Reaction #337334
titled product
收率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C(O)COc2ccc(C=O)cc2)nc1
Reaction #337335
4-[2-(5-ethyl-pyridin-2-yl)-2-hydroxy-ethoxy]-benzaldehyde
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C(O)COc2ccc(C=O)cc2)nc1
Reaction #337336
4-[2-(5-ethyl-pyridin-2-yl)-2-hydroxy-ethoxy]-benzaldehyde
收率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C(O)COc2ccc(C=O)cc2)nc1
Reaction #337337
titled product
收率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C(O)COc2ccc(C=O)cc2)nc1
Reaction #337338
4-[2-(5-ethyl-pyridin-2-yl)-2-hydroxy-ethoxy]-benzaldehyde
收率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C(O)CO)nc1
Reaction #337341
1-(5-ethyl-pyridin-2-yl)-ethan-1,2-diol
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C2COS(=O)O2)nc1
Reaction #337342
titled product
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C(O)COc2ccc(C=O)cc2)nc1
Reaction #337343
desired product
收率 48.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C(Cl)COc2ccc(C=O)cc2)nc1
Reaction #337344
desired product
收率 76.7%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C(Br)COc2ccc(C=O)cc2)nc1
Reaction #337345
desired product
收率 89.8%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C(COc2ccc(C=O)cc2)S(C)(=O)=O)nc1
Reaction #337348
desired product
收率 342.8%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C(COc2ccc(C=O)cc2)S(=O)(=O)c2ccc(C)cc2)nc1
Reaction #337350
desired product
DOI: 10.6084/m9.figshare.5104873.v1
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