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C1CCCC(=O)CC1

CCOC1(OCC)CC2C(=O)CCC21
Reaction #43462
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2C(O)CCC12
Reaction #43463
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CCC2C(=O)CC12)c1ccccc1
Reaction #43464
title compound
Выход 86.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2CCC(C1)N2
Reaction #44774
8-azabicyclo[3.2.1]octan-3-one
Выход 128.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN2C3CCC2CC(=O)C3)cc1
Reaction #44775
methyl 4-[(3-oxo-8-azabicyclo[3.2.1]oct-8-yl)methyl]-benzoate
Выход 75.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CNC2CC3CCC(C2)N3C(=O)OC(C)(C)C)cc1
Reaction #44780
1,1-dimethylethyl 3-[[[4-(methoxycarbonyl)phenyl]methyl]amino]-8-azabicyclo[3.2.1]octane-8-carboxylate
Выход 88.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=NO)C2CCC(C2)C1Cc1ccccn1
Reaction #51410
2-aza-2-benzyl-4-oximino-3-oxobicyclo[3.2.1]octane
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NC1C(=O)C(Cc2ccccn2)C2CCC1C2
Reaction #51411
title compound
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2CCC(C1)N2Cc1ccccc1
Reaction #52207
title compound
Выход 46.6%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #56795
N-benzyltropanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2CCC(C1)N2Cc1ccccc1
Reaction #56800
title intermediate
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CN2C3CCC2CC2(CO2)C3)cc1
Reaction #68978
8-Benzyl-spiro[8-azabicyclo[3.2.1]octane-3,2′-oxirane]
DOI: 10.6084/m9.figshare.5104873.v1
Cc1sc(-c2ccc(C(=O)O)cc2)cc1C1C(=O)C2CCC(C2)C1=O
Reaction #74184
4-[4-(2,4-dioxobicyclo[3.2.1]oct-3-yl)-5-methylthiophen-2-yl]benzoic acid
Выход 77.6%DOI: 10.6084/m9.figshare.5104873.v1
CCc1sc(-c2ccc(Cl)cc2)nc1C1=C(OC(=O)C(C)(C)C)C2CCC(C2)C1=O
Reaction #74189
2,2-dimethylpropionic acid 3-[2-(4-chlorophenyl)-5-ethylthiazol-4-yl]-4-oxobicyclo[3.2.1]oct-2-en-2-yl ester
Выход 81.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC2CCC3CCC1C32
Reaction #78831
2-oxatricyclo[5.2.1.04,10]decane-3-one
Выход 617.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1(CC#N)CCCCCC1=O
Reaction #93899
1-methyl-2-oxocycloheptaneacetonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C2CCC1CC(N)C2
Reaction #159324
tert-butyl 3-amino-8-azabicyclo[3.2.1]octane-8-carboxylate
Выход 98.9%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(Cl)cc2)cc1C1C(=O)C2CCC(C2)C1=O
Reaction #159434
3-(4′-chloro-4-ethylbiphen-3-yl)bicyclo[3.2.1]octane-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(Cl)cc2Cl)cc1C1C(=O)C2CCC(C2)C1=O
Reaction #159445
3-(2′,4′-dichloro-4-ethylbiphen-3-yl)bicyclo[3.2.1]octane-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(Cl)c(C)c2)cc1C1C(=O)C2CCC(C2)C1=O
Reaction #159446
3-(4′-chloro-4-ethyl-3′-methylbiphen-3-yl)bicyclo[3.2.1]octane-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
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