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653658

O=C(Nc1cccnc1)c1c(O)c2sccc2[nH]c1=O
Reaction #282620
DOI: 10.1039/C8SC04228D
C#CC(C)(C)NC(=O)c1c(O)c2sccc2[nH]c1=O
Reaction #320613
6- [(1,1-Dimethylpropinyl-)aminocarbonyl-]-7-hydroxy-thieno[3,2-b]pyridin-5(4H)-one
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)c(C(=O)NCC(=O)O)c(O)c2sccc21
Reaction #380455
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(O)c2sccc2n(N=Cc2ccccc2)c1=O
Reaction #688397
title compound
Выход 35.0%DOI: 10.6084/m9.figshare.5104873.v1
Nn1c(=O)c(C2=NS(=O)(=O)c3ccccc3N2)c(O)c2sccc21
Reaction #688398
title compound
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2c(O)c(C(=O)NCC(=O)O)c(=O)n(C)c12
Reaction #897383
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(Cl)c2sccc2n(Cc2cccc(F)c2)c1=O
Reaction #906008
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(Cl)c2sccc2[nH]c1=O
Reaction #989662
7-chloro-5-oxo-4,5-dihydro-thieno[3,2-b]pyridine-6-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(O)c2sccc2[nH]c1=O
Reaction #989664
7-hydroxy-5-oxo-4,5-dihydro-thieno[3,2-b]pyridine-6-carboxylic acid ethyl ester
Выход 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(O)c2sccc2n(Cc2cccc(F)c2)c1=O
Reaction #989674
4-(3-fluoro-benzyl)-7-hydroxy-5-oxo-4,5-dihydro-thieno[3,2-b]pyridine-6-carboxylic acid ethyl ester
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1c(O)c2sccc2n(Cc2cccc(F)c2)c1=O
Reaction #989675
4-(3-fluoro-benzyl)-7-hydroxy-5-oxo-4,5-dihydro-thieno[3,2-b]pyridine-6-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)c2sccc2n(Cc2cccc(F)c2)c1=O
Reaction #989676
7-chloro-4-(3-fluoro-benzyl)-5-oxo-4,5-dihydro-thieno[3,2-b]pyridine-6-carboxylic acid ethyl ester
Выход 88.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(O)c2sccc2n(Cc2ccc(OC)cc2)c1=O
Reaction #989699
7-hydroxy-4-(4-methoxybenzyl)-5-oxo-4,5-dihydro-thieno[3,2-b]pyridine-6-carboxylic acid ethyl ester
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)c2sccc2n(Cc2ccc(OC)cc2)c1=O
Reaction #989700
7-chloro-4-(4-methoxybenzyl)-5-oxo-4,5-dihydro-thieno[3,2-b]pyridine-6-carboxylic acid ethyl ester
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)c2sccc2n(Cc2ccc(OC)cc2)c1=O
Reaction #1630109
DOI: 10.1039/C8SC04228D
O=C(Nc1cccnc1)c1c(O)c2sccc2[nH]c1=O
Reaction #1674894
Compound 1
Выход 54.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccncc1)c1c(O)c2sccc2[nH]c1=O
Reaction #1674895
Compound 2
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)c(C(=O)NCC(=O)O)c(O)c2sccc21
Reaction #1748672
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2c(O)c(C(=O)NCC(=O)O)c(=O)n(C)c12
Reaction #1748673
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(O)c2sc(Br)c(C)c2n(C)c1=O
Reaction #1748674
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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