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Clc1ccc2ccccc2n1

O=C1OCc2c1c(Cl)nc1ccccc21
Reaction #5226
4-Chloro-furo[3,4-c]quinolin-3(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCc2c1cnc1ccccc21
Reaction #5227
Furo[3,4-c]quinolin-3(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
C(=C1CCCC1)c1cnc2ccccc2c1
Reaction #6006
3-cyclopentylidenemethylquinoline
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1c2c(cc3nc(Cl)ccc13)C1CNCC2C1)C(F)(F)F
Reaction #10207
1-(6-Chloro-5,14-diazatetracyclo[10.3.1.02,11.04,9]hexadeca-2(11),3,5,7,9-pentaen-10-yl)-2,2,2-trifluoro-ethanone
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C(=O)OC(C)(C)C)c3c(cc2n1)C1CNCC3C1
Reaction #10208
6-Methoxy-5,14-diazatetracyclo[10.3.1.02,11.04,9]hexadeca-2(11),3,5,7,9-pentaen-10-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NC(=O)c1cc(Cl)nc2ccccc12
Reaction #75726
2-chloroquinoline-4-carbonyl azide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc(F)c(F)cc2nc1Cl
Reaction #83632
3-ethoxycarbonyl-6,7-difluoro-2-chloroquinoline
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc(F)c(F)cc2nc1N(C)CCC#N
Reaction #83633
3-ethoxycarbonyl-6,7-difluoro-2-(N-methyl-N-β-cyanoethylamino)quinoline
Ausbeute 100.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(-c2nc3ccc(O)cc3cc2C(F)(F)F)cc1
Reaction #84085
4-(6-hydroxy-3-(trifluoromethyl)quinolin-2-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc2nc(Cl)cc(F)c2c1
Reaction #84101
product
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
OCc1cc2cc(Br)ccc2nc1Cl
Reaction #156249
(6-bromo-2-chloroquinolin-3-yl)methanol
DOI: 10.6084/m9.figshare.5104873.v1
ClCc1cc2cc(Br)ccc2nc1Cl
Reaction #156250
6-bromo-2-chloro-3-(chloromethyl)quinoline
DOI: 10.6084/m9.figshare.5104873.v1
Clc1nc2ccc(Br)cc2cc1C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Cl-]
Reaction #156251
((6-bromo-2-chloroquinolin-3-yl)methyl)triphenylphosphonium chloride
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cc(OCc2cc3cc(Br)ccc3nc2Cl)ncn1
Reaction #156266
6-bromo-2-chloro-3-((6-(trifluoromethyl)pyrimidin-4-yloxy)methyl)quinoline
DOI: 10.6084/m9.figshare.5104873.v1
CC(O)c1cc2cccc(F)c2nc1Cl
Reaction #162532
1-(2-chloro-8-fluoroquinolin-3-yl)ethanol
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc2cccc(F)c2nc1Cl
Reaction #162533
1-(2-chloro-8-fluoroquinolin-3-yl)ethanone
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)c1cc2cccc(F)c2nc1Cl
Reaction #162534
(R)-1-(2-chloro-8-fluoroquinolin-3-yl)ethanol
Ausbeute 73.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1cc2cccc(F)c2nc1Cl)N1C(=O)c2ccccc2C1=O
Reaction #162535
(S)-2-(1-(2-chloro-8-fluoroquinolin-3-yl)ethyl)-isoindoline-1,3-dione
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)c1cc2ccc(F)cc2nc1Cl
Reaction #162539
1-(2-chloro-7-fluoroquinolin-3-yl)-ethanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc2ccc(F)cc2nc1Cl
Reaction #162540
1-(2-chloro-7-fluoroquinolin-3-yl)ethanone
Ausbeute 81.5%DOI: 10.6084/m9.figshare.5104873.v1
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