Impliqué dans 281 réactions

7525

c1ccc(OCc2ccc3ccccc3n2)cc1
Reaction #4468
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COC(=O)c1ccc(OCc2ccc3ccccc3n2)cc1
Reaction #62097
title compound
Rendement 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(=O)c1ccc(OCc2ccc3ccccc3n2)cc1
Reaction #62117
title compound
Rendement 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
c1ccc2nc(COc3ccc(-n4nccc4-c4ccncc4)cc3)ccc2c1
Reaction #62153
title compound
Rendement 69.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
c1ccc2nc(COc3ccc(-c4nncn4-c4ccncc4)cc3)ccc2c1
Reaction #62162
title compound
Rendement 64.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
NC(=O)c1ccc(OCc2ccc3ccccc3n2)cc1
Reaction #62166
title compound
Rendement 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cn1cc(-c2ccncc2)c(-c2ccc(OCc3ccc4ccccc4n3)cc2F)n1
Reaction #62178
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
c1ccc2nc(COc3ccc(-c4ncoc4-c4ccncc4)cc3)ccc2c1
Reaction #62195
title compound
Rendement 20.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1nc(-c2ccc(OCc3ccc4ccccc4n3)cc2)c(-c2ccncc2)o1
Reaction #62199
title compound
Rendement 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC1Cc2ccc(OCc3ccc4ccccc4n3)cc2C1=O
Reaction #65973
pure title compound
Rendement 84.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COc1c(C=O)cccc1-c1ccc2ccccc2n1
Reaction #65975
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COC(=O)CC1=C(C)Cc2ccc(OCc3ccc4ccccc4n3)cc21
Reaction #65991
desired product
Rendement 79.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
OCc1cccc(OCc2ccc3ccccc3n2)c1
Reaction #82810
3-(Quinolin-2-ylmethoxy)benzyl alcohol
Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1cc(C)cc(C(=O)c2c(C(C)C)c(=O)[nH]c(=O)n2Cc2ccc3ccccc3n2)c1
Reaction #173202
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC(CCCCCOCc1ccccc1)c1cccc(OCc2ccc3ccccc3n2)c1
Reaction #174144
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1nc(-c2ccc(OCc3ccc4ccccc4n3)cc2)c(-c2ccncc2)o1
Reaction #174600
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(C)(C)Cc1c(SC(C)(C)C)c2cc(OCc3ccc4ccccc4n3)ccc2n1Cc1ccc(Cl)cc1
Reaction #175551
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc2nc(COc3ccc(-c4ncoc4-c4ccncc4)cc3)ccc2c1
Reaction #178158
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCCCOCc1ccc2ccccc2n1
Reaction #182838
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Oc1ccc(OCc2ccc3ccccc3n2)cc1C1(c2ccccc2)CC2CCC1C2
Reaction #182938
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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