Teilstruktursuche

12566013

O=C1CCCCCO1.O=C1COCCO1
Reaction #2356
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCCCO1.O=C1COCCO1
Reaction #2357
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCCCO1.O=C1COCCO1
Reaction #2358
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCCCO1.O=C1COCCO1
Reaction #2359
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1
COCCOCOc1cc(C(O)C(=O)OC(c2ccccc2)c2ccccc2)cc(F)c1OCOCCOC
Reaction #2670
Diphenylmethyl [3-fluoro-4,5-bis-[(2-methoxy-ethoxy)-methoxy]-phenyl]-hydroxy-acetate
DOI: 10.6084/m9.figshare.5104873.v1
COCCOCOc1ccc(C[C@H](NC(=O)OC(C)(C)C)C(=O)OC)cc1
Reaction #5822
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc(C(F)(F)F)cc2)SC[C@H]1OC(C)=O
Reaction #6095
expected product
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc(C(F)(F)F)cc2)SC[C@H]1OC(C)=O
Reaction #6096
expected product
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOCCOCCOC(=O)C1CC1
Reaction #7072
title product
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](C)Oc1cc(Oc2ccc(S(C)(=O)=O)cc2)cc(C(=O)O)c1
Reaction #48776
desired compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](C)Oc1cc(Oc2ccc(S(C)(=O)=O)cc2)cc(C(=O)Nc2ccn(C(=O)OC(C)(C)C)n2)c1
Reaction #48780
title compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc2c(c1)OC(CNCCO)CO2
Reaction #67197
2-({[7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}AMINO)ETHANOL
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CN(CCn2c(=O)cc(C)c3ccc(OC)cc32)CCN1CCc1ccc2c(c1)OCCO2
Reaction #68084
ethyl 1-(2-(2,3-dihydro-1,4-benzodioxin-6-yl)ethyl)-4-(2-(7-methoxy-4-methyl-2-oxoquinolin-1(2H)-yl)ethyl)piperazine-2-carboxylate
Ausbeute 64.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C)cc(=O)n(CCN3CCN(CCc4ccc5c(c4)OCCO5)C(C(=O)O)C3)c2c1
Reaction #68085
1-(2-(2,3-dihydro-1,4-benzodioxin-6-yl)ethyl)-4-(2-(7-methoxy-4-methyl-2-oxoquinolin-1(2H)-yl)ethyl)piperazine-2-carboxylic acid
Ausbeute 63.7%DOI: 10.6084/m9.figshare.5104873.v1
CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCOCCN=[N+]=[N-])c2)C1
Reaction #73939
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C(C)=C/c1cc(F)c(Oc2ccc(S(=O)(=O)NCCOCCOCCOCCN=[N+]=[N-])cc2)c(F)c1
Reaction #73969
title compound
Ausbeute 47.1%DOI: 10.6084/m9.figshare.5104873.v1
CCN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCOCCN=[N+]=[N-])c2)C1
Reaction #73990
N-(2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethyl)-3-(6,8-dichloro-2-ethyl-1,2,3,4-tetrahydroisoquinolin-4-yl)benzenesulfonamide
Ausbeute 55.4%DOI: 10.6084/m9.figshare.5104873.v1
CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCOCCN=[N+]=[N-])c2)C1
Reaction #73995
N-(2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethyl)-3-(6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(NCCOCCOCCOCCN=[N+]=[N-])c2)C1
Reaction #73998
N-(2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethyl)-3-(6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)aniline
DOI: 10.6084/m9.figshare.5104873.v1
CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(NC(=O)NCCOCCOCCOCCN=[N+]=[N-])c2)C1
Reaction #73999
1-(2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethyl)-3-(3-(6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenyl)urea
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter