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80501

c1ccc(CN2CCC3(CC2)OCc2ccccc23)cc1
Reaction #179157
DOI: 10.1039/C8SC04228D
Clc1ccc2c(c1)C1(CCNCC1)OC2
Reaction #224557
DOI: 10.1039/C8SC04228D
OC1(c2ccccc2C(F)(F)F)CCN(Cc2ccccc2)CC1
Reaction #225323
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCC2(CC1)OC(c1ccccc1)c1ccccc12
Reaction #238505
DOI: 10.1039/C8SC04228D
O=C1OC2(CCN(Cc3ccccc3)CC2)c2ccc(Cl)cc21
Reaction #266988
DOI: 10.1039/C8SC04228D
c1ccc2c(c1)COC21CCNCC1
Reaction #289223
DOI: 10.1039/C8SC04228D
CCc1c(Br)cccc1C1=CCN(Cc2ccccc2)CC1
Reaction #295248
DOI: 10.1039/C8SC04228D
O=C1OC2(CCN(Cc3ccccc3)CC2)c2ccccc21
Reaction #338654
1′-benzyl-3H-spiro[isobenzofuran-1,4′-piperidin]-3-one
Ausbeute 20.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #338655
HCl
Ausbeute 484.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC2(CCN(Cc3ccccc3)CC2)c2cc(Cl)ccc21
Reaction #357230
sub-titled compound
Ausbeute 37.2%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc2c(c1)C1(CCN(Cc3ccccc3)CC1)OC2
Reaction #357231
sub-titled compound
Ausbeute 85.6%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc2c(c1)C1(CCNCC1)OC2
Reaction #357232
titled compound
Ausbeute 28.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC2(CCN(Cc3ccccc3)CC2)c2ccc(F)cc21
Reaction #357233
sub-titled compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2c(c1)COC21CCN(Cc2ccccc2)CC1
Reaction #357234
sub-titled compound
Ausbeute 77.5%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2c(c1)COC21CCNCC1
Reaction #357235
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC2(CCN(Cc3ccccc3)CC2)c2ccc(Cl)cc21
Reaction #357273
subtitled compound
Ausbeute 37.2%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc2c(c1)COC21CCN(Cc2ccccc2)CC1
Reaction #357274
subtitled compound
Ausbeute 95.1%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc2c(c1)COC21CCNCC1
Reaction #357275
titled compound
Ausbeute 44.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1c(Br)cccc1C1(O)CCN(Cc2ccccc2)CC1
Reaction #389424
DOI: 10.1039/C8SC04228D
CCc1ccc2c(c1)C1(CCN(Cc3ccccc3)CC1)OC2=O.Cl
Reaction #479988
compound
DOI: 10.6084/m9.figshare.5104873.v1
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