Substructure Search

4205

C#CCn1c(=O)[nH]c(=O)n(-c2cc(N3C(=O)C4=C(CCCC4)C3=O)c(F)cc2Cl)c1=O
Reaction #1579
title product
Yield 55.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1ccc(Cl)cc1F
Reaction #1580
title product
Yield 69.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CN1C(=O)C2=C(CCCC2)C1=O)C1(C)OCCO1
Reaction #10959
Ethyl 3-(1,3-dioxo-1,3,4,5,6,7-hexahydro-isoindol-2-yl)-2-(2-methyl-[1,3]dioxolan-2-yl)propionate
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
Yield 65.0%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
Yield 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
Yield 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
Yield 79.2%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
O=c1[nH][nH]c(=O)c2c1CCCC2
Reaction #70498
2,3,5,6,7,8-hexahydro-phthalazin-1,4-dione
Yield 96.0%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
Yield 55.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1ccc(Cl)cc1F
Reaction #80707
title product
Yield 69.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1=C(C(=O)Nc2ccc(Br)cc2F)CCCC1
Reaction #179240
DOI: 10.1039/C8SC04228D
C=CCOc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #196918
DOI: 10.1039/C8SC04228D
C#CCn1c(=O)sc2cc(F)c(N3C(=O)C4=C(CCCC4)C3=O)cc21
Reaction #212655
DOI: 10.1039/C8SC04228D
CCCCCOC(=O)COc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #212694
DOI: 10.1039/C8SC04228D
O=C(O)C1=C(C(=O)Nc2ccc(Cl)cc2F)CCCC1
Reaction #213148
DOI: 10.1039/C8SC04228D
CC1CCCC1Oc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #215718
N-{2-fluoro-4-chloro-5-(2-methylcyclopentyl)oxyphenyl}-3,4,5,6-tetrahydrophthalimide
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1cc(OC2CCCCC2)c(Cl)cc1F
Reaction #215719
N-(2-fluoro-4-chloro-5-cyclohexyloxyphenyl) 3,4,5,6-tetrahydrophthalimide
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Oc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #215728
N-(2-fluoro-4-chloro-5-methoxycarbonyloxyphenyl)-3,4,5,6-tetrahydrophthalimide
Yield 79.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(C(=O)OC)CCCC1
Reaction #215950
title compound
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1
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