1-azabicyclo[2.2.2]octan-3-one

O=C1C(=Cc2ccccc2Cl)N2CCC1CC2
Reaction #5074
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1CCN2CCC1CC2
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titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C1CN2CCC1C1(CO1)C2
Reaction #76779
spiro[1-azabicyclo[2.2.2]octane-3,2′-oxirane]
Ausbeute 83.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)(C)OC(=O)CC1(O)CN2CCC1CC2
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subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C=CC1(O)CN2CCC1CC2
Reaction #76782
title compound
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C1CN2CCC1C1(CO1)C2
Reaction #77876
spiro[1-azabicyclo[2.2.2]octane-3,2′-oxirane]
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CC(C)(C)OC(=O)CC1(O)CN2CCC1CC2
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subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C=CC1(O)CN2CCC1CC2
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title compound
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C1C(=Cc2cccnc2)N2CCC1CC2
Reaction #177163
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O=[N+]([O-])CC1(O)CN2CCC1CC2
Reaction #179189
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OC1C2CCN(CC2)C1Cc1cccnc1
Reaction #187045
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OC1(c2nccnc2Cl)CN2CCC1CC2
Reaction #187838
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N#CC1(O)CN2CCC1CC2
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O=[N+]([O-])c1ccc2[nH]cc(C3=CN4CCC3CC4)c2c1
Reaction #189261
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OC1C2CCN(CC2)C1C(c1ccccc1)c1cccnc1
Reaction #192051
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O=C1C(=Cc2ccccc2)N2CCC1CC2
Reaction #197646
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OC1(Cc2ccccc2F)CN2CCC1CC2
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OC1CN2CCC1CC2
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COc1ccc2cc(C3(O)CN4CCC3CC4)ccc2c1
Reaction #239647
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O=C1C(=Cc2ccoc2)N2CCC1CC2
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