بحث البنية الفرعية

CCOCCOCC

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
المردود 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
المردود 48.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOCCOCCOC(=O)C1CC1
Reaction #7072
title product
DOI: 10.6084/m9.figshare.5104873.v1
OC1(c2cc3c(CCc4ccccc4)cccc3s2)O[C@H](COCc2ccccc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #43684
2,3,4,6-tetra-O-benzyl-1-[4-(2-phenylethyl)benzo[b]-thiophene-2-yl]-D-glucopyranose
المردود 86.2%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@H](c2cc3c(CCc4ccccc4)cccc3s2)[C@H](O)[C@@H](O)[C@@H]1O
Reaction #43685
title compound
المردود 30.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOCCOC(=O)CCC(C)=O
Reaction #54170
2-Butoxyethyl Levulinate
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
المردود 47.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C(C)=C/c1cc(F)c(Oc2ccc(S(=O)(=O)NCCOCCOCCOCCN)cc2)c(F)c1
Reaction #73970
title compound
المردود 101.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)=Cc1cc(F)c(Oc2ccc(S(=O)(=O)NCCOCCOCCOCCNC(=O)NCCOCCOCCOCCNS(=O)(=O)c3ccc(Oc4c(F)cc(C=C(C)C(=O)OCC)cc4F)cc3)cc2)c(F)c1
Reaction #73971
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C/C(=C\c1cc(F)c(Oc2ccc(S(=O)(=O)NCCOCCOCCOCCN=[N+]=[N-])cc2)c(F)c1)C(=O)N=C(N)N
Reaction #73972
title compound
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
المردود 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
C=C1CN(CCOCCOCCO)N=N1.COc1cc(/C=C/C(=O)CC(=O)/C=C/c2ccc(O)c(OC)c2)ccc1O
Reaction #90866
Mono-2-(2-(2-(4-(methylene)-1H-1,2,3-triazol-1-yl)ethoxy)ethoxy)ethanol-curcumin
المردود 26.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(CCC(=O)OCCOCCO)OCCOCCO
Reaction #161321
2-(2-hydroxyethoxy)ethyl 4-(2-(2-hydroxyethoxy)ethoxy)pentanoate
المردود 23.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(O)c1ccc(Cl)c(NC(=O)c2ccc(OCC3CN(C)c4ccccc4O3)cc2Cl)c1
Reaction #178457
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NCCOCCOCCOCCOCCOCCN
Reaction #181013
DOI: 10.1039/C8SC04228D
CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCOCCN=[N+]=[N-])c2)C1
Reaction #190620
DOI: 10.1039/C8SC04228D
الصفحة 1التالي