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189153

CC(=O)Nc1ccc([C@H](CNCCOc2ccc(-c3csc(C)n3)cc2)O[Si](C)(C)C(C)(C)C)cn1
Reaction #77681
desired product
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc([C@@H](O)CNCCOc2ccc(-c3csc(C)n3)cc2)cn1
Reaction #77682
desired product
Выход 83.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(-c2ccc(OCCNC[C@H](O)c3ccc(N)nc3)cc2)cs1
Reaction #77683
desired product
Выход 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc([C@H](CNCCOc2ccc(-c3csc(C)n3)cc2)O[Si](C)(C)C(C)(C)C)cn1
Reaction #500494
desired product
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc([C@@H](O)CNCCOc2ccc(-c3csc(C)n3)cc2)cn1
Reaction #500495
desired product
Выход 83.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(-c2ccc(OCCNC[C@H](O)c3ccc(N)nc3)cc2)cs1
Reaction #500496
desired product
Выход 74.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(-c2ccc(OCCNCC(O)c3ccc(N)nc3)cc2)cs1
Reaction #912433
DOI: 10.1039/C8SC04228D
CC(=O)Nc1ccc(C(CNCCOc2ccc(-c3csc(C)n3)cc2)O[Si](C)(C)C(C)(C)C)cn1
Reaction #913768
DOI: 10.1039/C8SC04228D
CC(=O)Nc1ccc(C(O)CNCCOc2ccc(-c3csc(C)n3)cc2)cn1
Reaction #1025826
DOI: 10.1039/C8SC04228D
N#Cc1nc(-c2ccc(OCCN3CCCCC3)cc2)cs1
Reaction #1320260
DOI: 10.1039/C8SC04228D
N#Cc1nc(-c2ccc(OCCN3CCCCC3)cc2)cs1
Reaction #1743595
4-[4-[2-(piperidin-1-yl)ethyloxy]phenyl]-thiazole-2-carbonitrile
Выход 93.1%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1nc(-c2ccc(OCCN3CCCCC3)cc2)cs1
Reaction #2223858
DOI: 10.1039/C8SC04228D
N#Cc1nc(-c2ccc(OCCN3CCCCC3)cc2)cs1
Reaction #2298341
4-[4-[2-(piperidin-1-yl)ethyloxy]phenyl]-thiazole-2-carbonitrile
Выход 93.1%DOI: 10.6084/m9.figshare.5104873.v1