子结构搜索

2382

C#CCn1c(=O)[nH]c(=O)n(-c2cc(N3C(=O)C4=C(CCCC4)C3=O)c(F)cc2Cl)c1=O
Reaction #1579
title product
收率 55.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1ccc(Cl)cc1F
Reaction #1580
title product
收率 69.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1cc([N+](=O)[O-])c(Cl)cc1F
Reaction #1581
title product
收率 101.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #1582
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1cc(OC2CCCC2)c(Cl)cc1F
Reaction #49741
N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)-3,4,5,6-tetrahydrophthalimide
收率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1cc(OC2CCCC2)c(Cl)cc1F
Reaction #49742
N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)-3,4,5,6-tetrahydrophthalimide
收率 30.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1cc(OC2CCCC2)c(Cl)cc1F
Reaction #49743
N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)-3,4,5,6-tetrahydrophthalimide
收率 31.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCC1Oc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #49744
N-{2-fluoro-4-chloro-5-(2-methylcyclopentyl)oxyphenyl}-3,4,5,6-tetrahydrophthalimide
收率 98.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1cc(OC2CCCCC2)c(Cl)cc1F
Reaction #49745
N-(2-fluoro-4-chloro-5-cyclohexyloxyphenyl)-3,4,5,6-tetrahydrophthalimide
收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Oc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #49756
N-(2-fluoro-4-chloro-5-methoxycarbonyloxyphenyl)-3,4,5,6-tetrahydrophthalimide
收率 79.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1cc(O)c(Cl)cc1F
Reaction #49757
N-(2-fluoro-4-chloro-5-hydroxypheyl)-3,4,5,6-tetrahydrophthalimide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1c(F)cc(Cl)c2nc(Cl)sc12
Reaction #50001
N-(2,4-Dichloro-6-fluorobenzothiazol-7-yl)-3,4,5,6-tetrahydrophthalimide
DOI: 10.6084/m9.figshare.5104873.v1
C#CCn1c(=O)[nH]c(=O)n(-c2cc(N3C(=O)C4=C(CCCC4)C3=O)c(F)cc2Cl)c1=O
Reaction #80706
title product
收率 55.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1ccc(Cl)cc1F
Reaction #80707
title product
收率 69.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1cc([N+](=O)[O-])c(Cl)cc1F
Reaction #80708
title product
收率 101.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #80709
title product
DOI: 10.6084/m9.figshare.5104873.v1
C#CCn1c(=O)n(CC=C)c(=O)n(-c2cc(N3C(=O)C4=C(CCCC4)C3=O)c(F)cc2Cl)c1=O
Reaction #80710
title product
收率 55.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCOC(=O)COc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #173784
DOI: 10.1039/C8SC04228D
COCCNC(=O)C1=C(C(=O)Nc2cc(OC3CCCC3)c(Cl)cc2F)CCCC1
Reaction #176074
DOI: 10.1039/C8SC04228D
CC(C)Oc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #179327
DOI: 10.1039/C8SC04228D
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