Substructure Search

255893

NCC(O)C1Cc2ccccc2N1C(=O)OCc1ccccc1
Reaction #6327
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Cc2cc(F)ccc2N1
Reaction #43540
2,2-dimethyl-5-fluoroindoline
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([N+](=O)[O-])c(C2=CC(C)(C)CC(C)(C)C2)c1
Reaction #60491
title compound
Yield 34.3%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #60492
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)N1CC(=CN(C)C)C(=O)c2cc([N+](=O)[O-])ccc21
Reaction #63949
3-dimethylaminomethylene-6-nitro-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)N1CCC(=O)c2cc(N)ccc21
Reaction #63954
6amino-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline
Yield 90.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)OCN1C(=O)CCc2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)cc21
Reaction #71516
Compound 2B
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Oc1ccc(Cl)cc1)N1CCCc2cc(OCC=CCBr)ccc21
Reaction #77745
6-(4-Bromo-but-2-enyloxy)-3,4-dihydro-2H-quinoline-1-carboxylic acid 4-chloro-phenyl ester
Yield 57.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Oc1ccc(Cl)cc1)N1CCCc2cc(OCCCCBr)ccc21
Reaction #77746
6-(4-Bromo-butoxy)-3,4-dihydro-2H-quinoline-1-carboxylic acid 4-chloro-phenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Oc1ccc(Cl)cc1)N1CCCc2cc(OCCCCCBr)ccc21
Reaction #77747
6-(5-Bromo-pentyloxy)-3,4-dihydro-2H-quinoline-1-carboxylic acid 4-chloro-phenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C)CCCCOc1ccc2c(c1)CCCN2C(=O)Oc1ccc(Cl)cc1
Reaction #77748
6-[4-(Allyl-methyl-amino)-butoxy]-3,4-dihydro-2H-quinoline-1-carboxylic acid 4-chloro-phenyl ester
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCc2cc(OCCCCCBr)ccc21
Reaction #77751
6-(5-Bromo-pentyloxy)-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCc2cc(OCCCCCCBr)ccc21
Reaction #77752
6-(6-Bromo-hexyloxy)-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C)CCCCCOc1ccc2c(c1)CCCN2C(=O)OC(C)(C)C
Reaction #77753
6-[5-(Allyl-methyl-amino)-pentyloxy]-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester
Yield 72.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C)CCCCCCOc1ccc2c(c1)CCCN2C(=O)OC(C)(C)C
Reaction #77754
6-[6-(Allyl-methyl-amino)-hexyloxy]-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCCCOc1ccc2c(c1)CCCN2C(=O)Oc1ccc(Cl)cc1
Reaction #77763
6-(4-Diethylamino-butoxy)-3,4-dihydro-2H-quinoline-1-carboxylic acid 4-chloro-phenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCCCOc1ccc2c(c1)CCCN2C(=O)Oc1ccc(Br)cc1
Reaction #77765
6-(4-Diethylamino-butoxy)-3,4-dihydro-2H-quinoline-1-carboxylic acid 4-bromo-phenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C)CC=CCOc1ccc2c(c1)CCCN2C(=O)OCC
Reaction #77766
6-[4-(Allyl-methyl-amino)-but-2-enyloxy]-3,4-dihydro-2H-quinoline-1-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccc(Br)cc2[N+](=O)[O-])n(C2CCCC2)n1
Reaction #156291
5-(4-bromo-2-nitrophenyl)-1-cyclopentyl-3-methyl-1H-pyrazole
Yield 62.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CC(=O)c1ccc(Br)cc1[N+](=O)[O-]
Reaction #156292
1-(4-bromo-2-nitrophenyl)butane-1,3-dione
Yield 73.6%DOI: 10.6084/m9.figshare.5104873.v1
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