3-quinuclidinol

c1ccc(Cn2cnc3c(OC4CN5CCC4CC5)nccc32)cc1
Reaction #1010
title compound
Ausbeute 48.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(CSC2CN3CCC2CC3)cc1
Reaction #5208
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(O)/C=C/C(=O)O.O=C(c1cnc(OC2CN3CCC2CC3)nc1C(F)(F)F)N1CCS(=O)(=O)CC1
Reaction #67074
3-({5-[(1,1-dioxidothiomorpholin-4-yl)carbonyl]-4-(trifluoromethyl)pyrimidin-2-yl}oxy)quinuclidine fumarate
Ausbeute 50.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cn1c(-c2cccc(Cl)c2)nc2ccc(OC3CN4CCC3CC4)cc2c1=O
Reaction #164592
2-(3-chlorophenyl)-3-methyl-6-(quinuclidin-3-yloxy)quinazolin-4(3H)-one
Ausbeute 12.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Nc1ccc(-c2cnc(OC3CN4CCC3CC4)cn2)cc1)OCc1ccccc1
Reaction #177494
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
FC(F)(F)c1ccccc1OC1CN2CCC1CC2
Reaction #181593
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1c2ccccc2-c2ccc(OC3CN4CCC3CC4)cc21
Reaction #191411
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(OC1CN2CCC1CC2)C(Nc1ccccc1)c1ccc(Cl)cc1
Reaction #198476
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C#CCOC1CN2CCC1CC2
Reaction #199857
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Ic1ccc(OC2CN3CCC2CC3)cc1
Reaction #200393
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Ic1ccc(-c2ccc(OC3CN4CCC3CC4)cc2)cc1
Reaction #211582
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[Cl-]
Reaction #213826
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(OC1CN2CCC1CC2)C(O)(C#Cc1ccccc1)C1CCCCC1
Reaction #222884
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Brc1ccc(OC2CN3CCC2CC3)cc1
Reaction #222922
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
[Br-]
Reaction #226287
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(Nc1ccccc1)OC1CN2CCC1CC2
Reaction #226607
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cccc2c(C(=O)OC3CN4CCC3CC4)cnn12
Reaction #227936
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(OC1CN2CCC1CC2)C1(c2ccccc2)CCCCCC1
Reaction #229542
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(OC1CN2CCC1CC2)C(Nc1ccc(F)cc1)c1ccccc1
Reaction #232734
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1ccc2c(c1)[nH]c1cc(OC3CN4CCC3CC4)ccc12
Reaction #236777
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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