431 件の反応に参加

1331027

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Reaction #58917
oil
収率 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=[N+]([O-])c1ccc(CCc2nccs2)cc1
Reaction #58930
2-[2-(4-nitrophenyl)ethyl]-1,3-thiazole
収率 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC(=O)C(C(=O)OC)=C1SC=C[SH]1O
Reaction #65192
dimethyl 3-hydroxy-1,3-dithiol-2-ylidenemalonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=[N+]([O-])c1cccc(-c2nn3c(c2-c2ccncc2)SCC3O)c1
Reaction #66369
crude product
収率 72.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cccc(-c2nn3c(c2-c2ccncc2)SCC3O)c1
Reaction #66377
crude product
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC[C@@H]1c2nccn2-c2cnc(Cl)nc2N1C1CCCC1
Reaction #67617
(R)-3-chloro-5-cyclopentyl-6-ethyl-5,6-dihydroimidazo[1,2-f]pteridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Brc1cccc(Nc2nccs2)n1
Reaction #77418
titled compound
収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)c1cc[nH]c1N
Reaction #92052
desired material
収率 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1cccc(-c2nccn2-c2c(C(C)C)cc(Br)cc2C(C)C)c1
Reaction #92819
desired product
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
c1ccn2ccnc2c1
Reaction #94288
imidazo[1,2-a]pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
c1ccn2ccnc2c1
Reaction #94299
Imidazo[1,2-a]pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
Cn1cc(-c2ccc3nccn3n2)cn1
Reaction #156346
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=CCN1C=NCCC1
Reaction #174388
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C(=O)O)c1ccc(Nc2nccs2)cc1
Reaction #191909
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(C(F)(F)F)cc1NCC=O
Reaction #213284
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
FC(F)=C(F)CCSc1nccs1
Reaction #219275
2-[(3,4,4-trifluoro-3-butenyl)sulphanyl]-1,3-thiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
ClCC=NCc1ccccc1
Reaction #226704
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(C)c(NCC=O)c1C
Reaction #279728
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCc1ccc(F)cc1NCC=O
Reaction #302472
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Nc1nc(Cl)c2ccn(Cc3ccccc3)c2n1
Reaction #309246
7-benzyl-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
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