52 件の反応に参加

13528

CC1CCN(CC#Cc2cccc(F)c2)CC1
Reaction #6886
oil
収率 56.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)N1CCC(O)(c2cc(F)ccc2Sc2cccc(F)c2)CC1
Reaction #43509
1-tert-Butoxycarbonyl-4-[2-(3-fluoro-phenylsulfanyl)-5-fluoro-phenyl]-piperidine-4-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(C)(C)C(=O)Nc1ccc(C#Cc2cccc(F)c2)cn1
Reaction #68821
N-[5-(3-fluoro-phenylethynyl)-pyridin-2-yl]-2-methoxy-2-methyl-propionamide
収率 66.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=c1cc(N2CCOCC2)nc2n1CC[C@@H](C(F)(F)F)N2c1cccc(F)c1
Reaction #167789
(8S)-9-(3-fluorophenyl)-2-(morpholin-4-yl)-8-(trifluoromethyl)-6,7,8,9-tetrahydro-4H-pyrimido[1,2-a]pyrimidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(C)n1-c1ccn(-c2cccc(F)c2)n1
Reaction #170679
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)c1cncc(C#Cc2cccc(F)c2)c1
Reaction #202358
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCN(CC#Cc2cccc(F)c2)CC1
Reaction #222948
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)C(=O)Nc1cccc(C2CCN(Cc3cccc4c3ccn4-c3cccc(F)c3)CC2)c1
Reaction #226151
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)N1CC(Oc2cccc(F)c2)CC1C(=O)N1CCCN(C2CCC2)CC1
Reaction #240890
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)c1cncc(C#Cc2cccc(F)c2)c1
Reaction #255687
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=Cc1c(F)cccc1I
Reaction #374000
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1cc(C)c(C2C(=O)C3C4CC(c5cccc(F)c5)C(O4)C3C2=O)c(C)c1
Reaction #495040
(1RS,2SR,6RS,7SR,8RS)-8-(3-fluorophenyl)-4-(2,4,6-trimethylphenyl)-10-oxatricyclo-[5.2.1.02,6]decane-3,5-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
O=Cc1c(-c2cccc(F)c2)sc2ccccc12
Reaction #610296
desired compound
収率 76.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CC(C)(C)OC(=O)C#Cc1cccc(F)c1
Reaction #610298
desired compound
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
NC(c1cccc(F)c1)C1(N2CCCC2)CCC1
Reaction #647387
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
O=C(CCCCCCc1ccccc1)c1ncc(-c2cccc(F)c2)o1
Reaction #692797
title compound
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CCOC(=O)c1cncc(C#Cc2cccc(F)c2)c1
Reaction #693981
title compound
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
N#Cc1cncc(C#Cc2cccc(F)c2)c1
Reaction #694018
title compound
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CCOC(=O)c1cncc(C#Cc2cccc(F)c2)c1
Reaction #694110
title compound
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CCOC(=O)C(C(=O)OCC)c1cccc(F)c1
Reaction #714712
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
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