Substructure Search

CCc1ncccc1CO

CCc1ncccc1CO
Reaction #1781
2-ethyl-3 -hydroxymethylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ncccc1CCl
Reaction #1782
2-ethyl-3-chloromethylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1ncccc1CO
Reaction #1784
2-isopropyl-3-hydroxymethylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1ncccc1CCl
Reaction #1785
2-isopropyl-3-chloromethylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C2CC2)nc2ccccc2c1-c1ccc(F)cc1
Reaction #52049
methyl 2-cyclopropyl-4-(4′-fluorophenyl)quinoline-3-carboxylate
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C2CC2)nc2ccccc2c1-c1ccc(F)cc1
Reaction #52050
methyl 2-cyclopropyl-4-(4′-fluorophenyl)quinoline-3-carboxylate
Yield 90.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C2CC2)nc2ccccc2c1-c1ccc(F)cc1
Reaction #52051
methyl 2-cyclopropyl-4-(4′-fluorophenyl)quinoline-3-carboxylate
Yield 85.6%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1c(C2CC2)nc2ccccc2c1-c1ccc(F)cc1
Reaction #52559
4-(4′-fluorophenyl)-2-cyclopropylquinoline-3-carbaldehyde
Yield 77.9%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1c(C2CC2)nc2ccccc2c1-c1ccc(F)cc1
Reaction #52560
4-(4′-fluorophenyl)-2-cyclopropylquinoline-3-carbaldehyde
Yield 76.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C(C)C)nc(OC)c(CO)c1-c1ccc(F)cc1
Reaction #65195
Ethyl 4-(4-fluorophenyl)-3-hydroxymethyl-6-isopropyl-2-methoxy-pyridine-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccnc1C1CCN(C(=O)OC(C)(C)C)CC1
Reaction #69905
3′,4′,5′,6′-tetrahydro-2′H-[2,4]bipyridinyl-3,1′-dicarboxylic acid 1′-t-butyl ester 3-methyl ester
Yield 59.5%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(CC)c1-c1cc(C)c2c(n1)CC(C)OC2=O
Reaction #168006
2-(2,6-diethylphenyl)-4,7-dimethyl-7,8-dihydro-5H-pyrano[4,3-b]pyridin-5-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCc1c(C(C)C)nc(C(C)C)c(C(C)O)c1-c1ccc(F)cc1
Reaction #185451
DOI: 10.1039/C8SC04228D
CCCCCc1c(C(C)C)nc(C(C)C)c(C(O)CCCC)c1-c1ccc(F)cc1
Reaction #185917
DOI: 10.1039/C8SC04228D
OC1CCCc2nc3ccccc3c(NCc3ccccc3Cl)c21
Reaction #188604
DOI: 10.1039/C8SC04228D
COc1cc(OC)nc(C2OC(=O)c3c(-c4ccccc4)ccnc32)n1
Reaction #194077
DOI: 10.1039/C8SC04228D
CCCc1ncccc1CO
Reaction #197146
DOI: 10.1039/C8SC04228D
c1ccc(CONC2(Cc3ccccc3)CCCc3nc(OCc4ccccc4)ccc32)cc1
Reaction #197391
DOI: 10.1039/C8SC04228D
CCCC=Cc1c(C(C)C)nc(C(C)C)c(CO)c1-c1cccc(OCc2ccccc2)c1
Reaction #201476
DOI: 10.1039/C8SC04228D
CC(C)c1nc(C(C)C)c(CCc2ccccc2)c(-c2ccc(F)cc2)c1CO
Reaction #202748
DOI: 10.1039/C8SC04228D
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