Teilstruktursuche

389140

CCCC(=O)c1cnc2c(OCCSC)cccc2c1Nc1ccccc1CC
Reaction #226118
DOI: 10.1039/C8SC04228D
CCCC(=O)c1cnc2c(OCCS(C)=O)cccc2c1Nc1ccccc1C(C)C
Reaction #236525
DOI: 10.1039/C8SC04228D
CCCC(=O)c1cnc2c(OCCCN3CCCCC3)cccc2c1Nc1ccccc1C
Reaction #255390
DOI: 10.1039/C8SC04228D
CCCC(=O)c1cnc2c(OCCCN(C)C)cccc2c1Nc1ccc(F)cc1C
Reaction #267932
DOI: 10.1039/C8SC04228D
CCCC(=O)c1cnc2c(OCCSC)cccc2c1Nc1ccccc1C(C)C
Reaction #283772
DOI: 10.1039/C8SC04228D
CCCC(=O)c1cnc2c(OCCCN(C)CCCc3ccccc3)cccc2c1Nc1ccccc1C
Reaction #289512
DOI: 10.1039/C8SC04228D
CCCC(=O)c1cnc2c(OCCCN(C)Cc3ccccc3)cccc2c1Nc1ccccc1C
Reaction #300847
DOI: 10.1039/C8SC04228D
CCCC(=O)c1cnc2c(OC)cccc2c1Nc1c(C)cc(O)cc1C
Reaction #378095
DOI: 10.1039/C8SC04228D
CCCC(=O)c1cnc2c(OCCOC)cccc2c1Nc1ccccc1C
Reaction #378997
DOI: 10.1039/C8SC04228D
CCCC(=O)c1cnc2c(OCCCN3CCOCC3)cccc2c1Nc1ccccc1C
Reaction #379531
DOI: 10.1039/C8SC04228D
CCCC(=O)c1cnc2c(OC)cccc2c1Nc1ccc(OC(C)=O)cc1C
Reaction #382391
DOI: 10.1039/C8SC04228D
CCCC(=O)c1cnc2c(OC)cccc2c1Nc1c(C)cc2c(c1C)OCO2
Reaction #390561
DOI: 10.1039/C8SC04228D
CCOC(=O)CCC(O)c1cnc2c(OC)cccc2c1Nc1ccccc1C
Reaction #397303
DOI: 10.1039/C8SC04228D
CCCCCC(=O)c1cnc2c(OC)cccc2c1Nc1ccccc1C
Reaction #777780
DOI: 10.1039/C8SC04228D
CCCC(=O)c1cnc2c(OC)cccc2c1Nc1cc(CO)ccc1C
Reaction #782778
DOI: 10.1039/C8SC04228D
CCCC(=O)c1cnc2c(OCCSC)cccc2c1Nc1ccccc1C
Reaction #830285
3-butyryl-4-(2-methylphenylamino)-8-(2-methylthioethoxy)quinoline
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)c1cnc2c(OCCS(C)=O)cccc2c1Nc1ccccc1C
Reaction #830286
desired product
Ausbeute 43.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)c1cnc2c(OCCSC)cccc2c1Nc1ccccc1C(C)C
Reaction #830287
desired product
Ausbeute 80.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)c1cnc2c(OCCS(C)=O)cccc2c1Nc1ccccc1C(C)C
Reaction #830288
desired product
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)c1cnc2c(OCCSC)cccc2c1Nc1ccc(F)cc1C
Reaction #830292
desired product
Ausbeute 11.8%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter