pyrrole

O=C(c1ccc[nH]1)C(Cl)(Cl)Cl
Reaction #1223
2-trichloroacetylpyrrole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
FC(F)(F)C(c1ccc[nH]1)c1ccc[nH]1
Reaction #1401
bis(pyrrol-2-yl)trifluoromethylmethane
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC(c1ccc[nH]1)c1ccc[nH]1
Reaction #7041
1,1-di-(2-pyrryl)-butane
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cn1c(-c2ccc(Cn3cccc3)cc2)cc2onc(-c3ccccc3)c2c1=O
Reaction #8409
desired compound
収率 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=S(=O)(c1ccccc1)n1cccc1
Reaction #11332
1-benzenesulfonylpyrrole
収率 736.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)c1ccc[nH]1
Reaction #47194
tert-butylpyrrole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C1=Cc2cc3ccc(cc4nc(cc5ccc(cc1n2)[nH]5)C=C4)[nH]3
Reaction #48476
porphine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(S(=O)(=O)n2cccc2)nn1
Reaction #51032
3-methoxy-6-(pyrrole-1-sulfonyl)-pyridazine
収率 30.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
c1c[nH]c(CN2CCOCC2)c1
Reaction #72528
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(c1ccc[nH]1)C(Cl)(Cl)Cl
Reaction #72533
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=[N+]([O-])c1ccc(-n2cccc2)c(F)c1
Reaction #84406
title compound
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1ccc(-c2c3nc(c(-c4ccccc4)c4ccc([nH]4)c(-c4ccccc4)c4nc(c(-c5ccccc5)c5ccc2[nH]5)C=C4)C=C3)cc1
Reaction #93822
4-(10,15,20-triphenyl-21H,23H-porphin- 5-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CC(=O)OCCn1cccc1
Reaction #95387
1-(2-acetoxyethyl)pyrrole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
C[S+](C)c1ccc[nH]1.[Cl-]
Reaction #96169
dimethyl 2-pyrrolylsulfonium chloride
収率 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
N#Cc1c[nH]c(C#N)c1
Reaction #160846
above compound
収率 73.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)OCCn1cccc1
Reaction #177865
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSCC1C2OC(C)(C)OC2C(c2c[nH]c(C#N)c2N)N1C(=O)OC(C)(C)C
Reaction #178043
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1ccc[nH]1)C(Cl)(Cl)Cl
Reaction #180226
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=S(=O)(c1ccc(C(F)(F)F)cc1)n1cccc1
Reaction #180574
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=S(=O)(c1ccccc1)n1cccc1
Reaction #183724
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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