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Brc1cnc2c(c1)CC1(CN3CCC1CC3)O2
Reaction #76784
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2cnc3c(c2)CC2(CN4CCC2CC4)O3)cc1
Reaction #76785
title compound
Ausbeute 68.5%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2c(c1)CC1(CN3CCC1CC3)O2
Reaction #76786
title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2c(c1)C[C@@]1(CN3CCC1CC3)O2
Reaction #76787
title compound
Ausbeute 98.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cnc2c(c1)CC1(CN3CCC1CC3)O2
Reaction #76788
amine
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cnc2c(c1)C[C@]1(CN3CCC1CC3)O2
Reaction #76789
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)Nc1cnc2c(c1)CC1(CN3CCC1CC3)O2
Reaction #76790
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1cnc2c(c1)CC1(CN3CCC1CC3)O2
Reaction #76791
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
C(=C\c1cnc2c(c1)C[C@]1(CN3CCC1CC3)O2)/c1ccccc1
Reaction #76792
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
c1nc2c(cc1N1CCC1)C[C@@]1(CN3CCC1CC3)O2
Reaction #76793
(R)-(−)-5′-(1-Azetidinyl)spiro[1-azabicyclo[2.2.2]octane-3,2′(3′H)-furo[2,3-b]pyridine]
DOI: 10.6084/m9.figshare.5104873.v1
C(=Cc1ccccn1)c1cnc2c(c1)C[C@@]1(CN3CCC1CC3)O2
Reaction #76794
title compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)C#Cc1cnc2c(c1)C[C@@]1(CN3CCC1CC3)O2
Reaction #76795
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cnc2c(c1)C[C@@]1(CN3CCC1CC3)O2
Reaction #76796
title compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
c1coc(-c2cnc3c(c2)CC2(CN4CCC2CC4)O3)c1
Reaction #76797
title compound
Ausbeute 89.2%DOI: 10.6084/m9.figshare.5104873.v1
c1cncc(-c2cnc3c(c2)CC2(CN4CCC2CC4)O3)c1
Reaction #76798
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc2c(c1)CC1(CN3CCC1CC3)O2
Reaction #76799
title compound
Ausbeute 166.3%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cnc2c(c1)CC1(CN3CCC1CC3)O2
Reaction #76800
title compound
Ausbeute 186.9%DOI: 10.6084/m9.figshare.5104873.v1
Brc1cnc2c(c1)CC1(CN3CCC1CC3)O2
Reaction #77881
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2cnc3c(c2)CC2(CN4CCC2CC4)O3)cc1
Reaction #77882
title compound
Ausbeute 68.5%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2c(c1)CC1(CN3CCC1CC3)O2
Reaction #77883
title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
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