Участвует в 57 реакциях

2321

N#Cc1ccc(C=O)s1
Reaction #1691
2-cyano-5-formyl-thiophene
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1cc([N+](=O)[O-])cs1
Reaction #63793
4-nitro-2-cyanothiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CS(=O)(=O)c1ccc(NC(=N)c2cccs2)cc1
Reaction #80637
N-[4-(methylsulfonyl) phenyl]-2-thiophenecarboximidamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C1NC(c2cccs2)=C2C(=O)NC(c3cccs3)=C12
Reaction #171154
3,6-bis(thiophen-2-yl)-2H,5H-pyrrolo[3,4-c]pyrrole-1,4-dione
Выход 82.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NC(=NO)c1cccs1
Reaction #180842
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N=C(NO)c1cccs1
Reaction #186174
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N=C(NO)c1cccs1
Reaction #190876
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccc(SC[N+](=O)[O-])s1
Reaction #224289
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(c1ccc(CO)cc1)c1cccs1
Reaction #346087
α-hydroxy-p-tolyl 2-thienyl ketone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
CC(=O)c1cccc(C(=O)c2cccs2)c1C
Reaction #346092
2'-methyl-3'-(2-thenoyl)acetophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
CC(O)c1ccc(C(=O)c2cccs2)cc1
Reaction #346106
p-(1-hydroxyethyl)phenyl 2-thienyl ketone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
N#Cc1ccc(C=O)s1
Reaction #394356
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
N=C(Nc1ncc(Br)nc1Br)c1cccs1
Reaction #399333
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=N)c1cccs1
Reaction #414316
methyl 2-thiophenecarboximidate
Выход 817.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
COC(=N)c1cccs1
Reaction #461375
methyl 2-thiophenecarboximidate
Выход 817.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
N#Cc1ccc(C=O)s1
Reaction #519856
2-cyano-5-formylthiophene
Выход 55.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
O=C(c1ccc(CO)cc1)c1cccs1
Reaction #548899
α-hydroxy-p-tolyl 2-thienyl ketone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_12
CC(O)c1ccc(C(=O)c2cccs2)cc1
Reaction #548917
p-(1-hydroxyethyl)phenyl 2-thienyl ketone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_12
NC(=NO)c1cccs1
Reaction #549352
product
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_12
O=C1NC(c2cccs2)=C2C(=O)NC(c3cccs3)=C12
Reaction #555889
2,5-dihydro-1,4-dioxo-3,6-dithienylpyrrolo[3,4-c]-pyrrole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
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