1,3-cyclohexandione

CC1(C)COC2(CCCC(=O)C2)OC1
Reaction #3712
3,3-dimethyl-1,5-dioxa-spiro[5,5]undecan-8-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OC1=CC(=NNc2ccc(F)cc2)CCC1
Reaction #4470
title compound
収率 96.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C1CCCC(=NNc2ccc(Br)cc2)C1
Reaction #4472
1,3-Cyclohexanedione mono(4-bromophenylhydrazone)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COc1ccc2[nH]c3c(c2c1)C(=O)CCC3
Reaction #4475
title compound
収率 48.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C1CCCc2[nH]c3ccc(OCc4ccccc4)cc3c21
Reaction #4478
title compound
収率 38.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
N#Cc1ccccc1NC1=CC(=O)CCC1
Reaction #6316
2-(3-oxocyclohexen-1-yl)aminobenzonitrile
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CN(C)C=C1C(=O)CCCC1=O
Reaction #50545
2-dimethylaminomethylene-1,3-cyclohexanedione
収率 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=C1C=C(OCc2ccccc2)CCC1
Reaction #51876
title compound
収率 69.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(O)CCc1c[nH]c2c1C(=O)CCC2
Reaction #52615
3-(4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)-propionic acid
収率 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CS(=O)(=O)c1ccc(C(=O)OC2=CC(=O)CCC2)c(Cl)c1C1=NOC2OCCC12
Reaction #76422
3-Oxocyclohex-1-enyl 2-chloro-4-methylsulfonyl-3-(3a,4,5,6a-tetra-hydrofuro[3,2-d]isoxazol-3-yl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCS(=O)(=O)c1ccc(C(=O)OC2=CC(=O)CCC2)c(Cl)c1C1=NOC2OCCC12
Reaction #76423
3-Oxocyclohex-1-enyl 2-chloro-4-ethylsulfonyl-3-(3a,4,5,6a-tetrahydrofuro[3,2-d]isoxazol-3-yl)-benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COC(=O)c1cccc(NC2=CC(=O)CCC2)c1Cl
Reaction #79624
3-(3-carbomethoxy-2-chloroanilino)cyclohex-2-en-1-one
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COC(=O)c1cccc(NC2=CC(=O)CCC2)c1Br
Reaction #79628
3-(3-carbomethoxy-2-bromoanilino)cyclohex-2-en-1-one
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC1=CC(c2ccc(Cl)cc2)C2=C(CCCC2=O)N1
Reaction #82706
title compound
収率 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC1=CC(c2cccc(C(F)(F)F)c2)C2=C(CCCC2=O)N1
Reaction #82707
title compound
収率 39.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC1=CC(c2ccc(C(F)(F)F)cc2)C2=C(CCCC2=O)N1
Reaction #82708
title compound
収率 56.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC1=CC(c2cccc(Cl)c2)C2=C(CCCC2=O)N1
Reaction #82709
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC1=CC(c2ccc(C)cc2)C2=C(CCCC2=O)N1
Reaction #82710
title compound
収率 25.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C1CCCC2=C1C(c1cccc([N+](=O)[O-])c1)C1=C(CCCC1)N2
Reaction #82711
title compound
収率 7.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(C)CC1=CC(c2ccccc2)C2=C(CCCC2=O)N1
Reaction #82714
title compound
収率 19.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
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