Teilstruktursuche

239268

Cc1nc(Cl)c(C=O)c2c1CCCC2
Reaction #182361
DOI: 10.1039/C8SC04228D
CC(=O)C=Cc1c(Cl)nc(C)c2c1CCCC2
Reaction #185579
DOI: 10.1039/C8SC04228D
CCc1cnc(Cl)c(C(O)C2=CCCC2=O)c1
Reaction #191694
DOI: 10.1039/C8SC04228D
CCCCc1cnc(Cl)c(C(=O)O)c1
Reaction #228888
DOI: 10.1039/C8SC04228D
CCc1cnc(Cl)c(C(=O)NC(=N)COCCc2cc(F)ccc2F)c1
Reaction #234143
DOI: 10.1039/C8SC04228D
CCc1cnc(Cl)c(C(=O)NC(=N)COCCc2cccc(Cl)c2)c1
Reaction #281590
DOI: 10.1039/C8SC04228D
Cc1nc(Cl)c(C=O)c2c1CCCC2
Reaction #322774
3-Chloro-1-methyl-5,6,7,8-tetrahydroisoquinoline-4-carboxaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C=Cc1c(Cl)nc(C)c2c1CCCC2
Reaction #322778
1-(3-chloro-1-methyl-5,6,7,8-tetrahydroisoquinolin-4-yl)-but-1-en-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(C(=O)OC)c(OC)nc1C
Reaction #360861
pure product
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(CC)nc2c(c1O)C(=O)CC(C)(C)C2
Reaction #660884
Ethyl 2-ethyl-4-hydroxy-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydroquinoline-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C2=CCOCC2)nc2c(c1O)C(=O)CC1(CCC1)C2
Reaction #660924
Ethyl 2′-(3,6-dihydro-2H-pyran-4-yl)-4′-hydroxy-5′-oxo-6′,8′-dihydro-5′H-spiro[cyclobutane-1,7′-quinoline]-3′-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Cc2nc(Cl)c3c(c2[C@@H](O[Si](C)(C)C(C)(C)C)C1)C1(CCOCC1)OC3(O)c1ccc(C(F)(F)F)cc1
Reaction #660971
(9S)-9-(tert-Butyldimethylsilyloxy)-4-chloro-7,7-dimethyl-3-(4-(trifluoromethyl)phenyl)-2′,3′,5′,6,6′,7,8,9-octahydro-3H-spiro[furo[3,4-c]quinoline-1,4′-pyran]-3-ol
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Cc2nc(Cl)c3c(c2[C@@H](O[Si](C)(C)C(C)(C)C)C1)C1(CCOCC1)OC3=O
Reaction #660972
(S)-9-(tert-Butyldimethylsilyloxy)-4-chloro-7,7-dimethyl-2′,3′,5′,6,6′,7,8,9-octahydro-3H-spiro[furo[3,4-c]quinoline-1,4′-pyran]-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Cc2nc(Cl)c3c(c2[C@@H](O)C1)C1(CCOCC1)OC3=O
Reaction #660973
(S)-4-Chloro-9-hydroxy-7,7-dimethyl-2′,3′,5′,6,6′,7,8,9-octahydro-3H-spiro[furo[3,4-c]quinoline-1,4′-pyran]-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)c2c(nc(Cl)c3c2C2(CCOCC2)OC3=O)C1
Reaction #660974
4-Chloro-7,7-dimethyl-2′,3′,5′,6′,7,8-hexahydro-3H-spiro[furo[3,4-c]quinoline-1,4′-pyran]-3,9(6H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cnc(Cl)c(C(=O)NC(=N)COCCc2ccc(F)c(Cl)c2)c1
Reaction #895287
DOI: 10.1039/C8SC04228D
NC(=O)c1cc(C2CC2)c(Cl)nc1Cl
Reaction #1107991
2,6-dichloro-5-cyclopropylnicotinamide
Ausbeute 838.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CCCOc1nc(Cl)c(C2CC2)cc1C(N)=O
Reaction #1108001
6-chloro-5-cyclopropyl-2-(4-oxopentyloxy)nicotinamide
Ausbeute 19.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OCCOc1nc(Cl)c(C2CC2)cc1C(N)=O
Reaction #1108004
6-chloro-5-cyclopropyl-2-(2-isopropoxyethoxy)nicotinamide
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C(=O)OCC)C(O)c1cc(CC)cnc1Cl
Reaction #1209679
DOI: 10.1039/C8SC04228D
Seite 1Weiter