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NCC1(O)CCSCC1

O=[N+]([O-])CC1(O)CCSCC1
Reaction #73048
4-(nitromethyl)tetrahydro-2H-thiopyran-4-ol
Выход 42.7%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1c(Cl)nc2ccccc2c1NCC1(O)CCSCC1
Reaction #73049
4-{[(2-chloro-3-nitroquinolin-4-yl)amino]methyl}tetrahydro-2H-thiopyran-4-ol
Выход 59.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)Nc1c(Cl)nc2ccccc2c1NCC1(O)CCSCC1
Reaction #73050
N-(2-chloro-4-{[(4-hydroxytetrahydro-2H thiopyran-4-yl)methyl]amino}quinolin-3-yl)butanamide
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1c(Cl)nc2ccccc2c1NCC1(O)CCSCC1
Reaction #192823
DOI: 10.1039/C8SC04228D
CC(C)(C)Cn1c(CN2C(=O)OC3(CCSCC3)C2=O)cc2cnc(C#N)nc21
Reaction #358796
7-(2,2-dimethyl-propyl)-6-(2,4-dioxo-1-oxa-8-thia-3-aza-spiro[4.5]dec-3-ylmethyl)-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile
Выход 39.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)Cn1c(CN2C(=O)OC3(CCSCC3)C2=O)cc2cnc(C#N)nc21
Reaction #786227
DOI: 10.1039/C8SC04228D
O=[N+]([O-])CC1(O)CCSCC1
Reaction #1450790
4-(nitromethyl)tetrahydro-2H-thiopyran-4-ol
Выход 42.7%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1c(Cl)nc2ccccc2c1NCC1(O)CCSCC1
Reaction #1450791
4-{[(2-chloro-3-nitroquinolin-4-yl)amino]methyl}tetrahydro-2H-thiopyran-4-ol
Выход 59.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)Nc1c(Cl)nc2ccccc2c1NCC1(O)CCSCC1
Reaction #1450792
N-(2-chloro-4-{[(4-hydroxytetrahydro-2Hthiopyran-4-yl)methyl]amino}quinolin-3-yl)butanamide
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])CC1(O)CCSCC1
Reaction #1556493
4-(nitromethyl)tetrahydro-2H-thiopyran-4-ol
Выход 42.7%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1c(Cl)nc2ccccc2c1NCC1(O)CCSCC1
Reaction #1556494
4-{[(2-chloro-3-nitroquinolin-4-yl)amino]methyl}tetrahydro-2H-thiopyran-4-ol
Выход 59.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)Nc1c(Cl)nc2ccccc2c1NCC1(O)CCSCC1
Reaction #1556495
N-(2-chloro-4-{[(4-hydroxytetrahydro-2Hthiopyran-4-yl)methyl]amino}quinolin-3-yl)butanamide
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])CC1(O)CCSCC1
Reaction #2398909
DOI: 10.1039/C8SC04228D