بحث البنية الفرعية

11560

CNC(=O)c1c(I)c(N=C=O)c(I)c(C(=O)N(C)C)c1I
Reaction #56267
3-acetamido-5-{3-[2-D-gluco-2-deoxy-3,4,5,6-tetrahydroxy-1-oxohexyl]ureido}-2,4,6-triiodo-N-methylbenzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOCOC(=O)c1c(I)cc(I)c(NC(C)=O)c1I
Reaction #56528
product
المردود 32.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([N+](=O)[O-])c(C2=CC(C)(C)CC(C)(C)C2)c1
Reaction #60491
title compound
المردود 34.3%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCNC(=O)c1cc(I)c(NC(=O)c2ccc3c(c2)OCO3)cc1OC
Reaction #60571
Benzo[1,3]dioxole-5-carboxylic acid [4-(2-diethylamino-ethylcarbamoyl)-2-iodo-5-methoxy-phenyl]-amide
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1cc2cc([N+](=O)[O-])c(C(F)(F)F)cc2n1S(C)(=O)=O
Reaction #61206
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCSCC(C)(OC)c1cc2cc([N+](=O)[O-])c(C(F)(F)F)cc2n1S(C)(=O)=O
Reaction #61209
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCSCC(O)c1cc2cc([N+](=O)[O-])c(C(F)(F)F)cc2n1S(C)(=O)=O
Reaction #61212
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(O)(CSCC(F)(F)F)c1cc2cc([N+](=O)[O-])c(C(F)(F)F)cc2n1S(C)(=O)=O
Reaction #61214
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1c(I)c(C(=O)OC(C)OC(=O)Oc2ccccc2)c(I)c(N(C)C(C)=O)c1I
Reaction #65063
1-(Phenyloxycarbonyloxy)ethyl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)OC(C)OC(=O)c1c(I)c(NC(C)=O)c(I)c(NC(C)=O)c1I
Reaction #65066
1-(Ethyloxycarbonyloxy)ethyl 3,5-di(acetylamino)-2,4,6-triiodobenzenecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(OC(=O)Oc1ccccc1)OC(=O)c1c(I)c(NC(C)=O)c(I)c(N(C)C(C)=O)c1I
Reaction #65069
1-(Phenyloxycarbonyloxy)pentyl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1c(I)c(C(=O)OC(OC(=O)Oc2ccccc2)c2ccccc2)c(I)c(N(C)C(C)=O)c1I
Reaction #65070
1-(Phenyloxycarbonyloxy)-1-phenylmethyl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C#CC(C)C)c([N+](=O)[O-])c1
Reaction #68408
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N(CC(O)CCCCC(O)CN(C(C)=O)c1c(I)c(C(=O)N(CCO)CCO)c(I)c(C(=O)N(CCO)CCO)c1I)c1c(I)c(C(=O)N(CCO)CCO)c(I)c(C(=O)N(CCO)CCO)c1I
Reaction #70106
expected product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N(CC(O)COCCOCC(O)CN(C(C)=O)c1c(I)c(C(=O)N(CCO)CCO)c(I)c(C(=O)N(CCO)CCO)c1I)c1c(I)c(C(=O)N(CCO)CCO)c(I)c(C(=O)N(CCO)CCO)c1I
Reaction #70107
expected product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N(CC(O)CCCCC(O)CN(C(C)=O)c1c(I)c(C(=O)NCC(O)CO)c(I)c(C(=O)NCC(O)CO)c1I)c1c(I)c(C(=O)NCC(O)CO)c(I)c(C(=O)NCC(O)CO)c1I
Reaction #70109
5,5′-(2,7-dihydroxyoctane-1,8-diyl)bis(acetylazanediyl)bis(N1,N3-bis(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamide)
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N(CC(O)CCCCC(O)CN(C(C)=O)c1c(I)c(C(=O)N(C)CC(O)CO)c(I)c(C(=O)N(C)CC(O)CO)c1I)c1c(I)c(C(=O)N(C)CC(O)CO)c(I)c(C(=O)N(C)CC(O)CO)c1I
Reaction #70110
5,5′-(2,7-dihydroxyoctane-1,8-diyl)bis(acetylazanediyl)bis(N1,N3-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-N1,N3-dimethylisophthalamide)
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N(CC(O)COCCOCC(O)CN(C(C)=O)c1c(I)c(C(=O)NCC(O)CO)c(I)c(C(=O)NCC(O)CO)c1I)c1c(I)c(C(=O)NCC(O)CO)c(I)c(C(=O)NCC(O)CO)c1I
Reaction #70111
5,5′-(5,12-dihydroxy-2,15-dioxo-7,10-dioxa-3,14-diazahexadecane-3,14-diyl)bis(N1,N3-bis(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamide)
المردود 7.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2CC(C(=O)O)Nc3c(I)cccc32)cc1OC
Reaction #75694
Compound 70
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1cc2cc([N+](=O)[O-])c(C(F)(F)F)cc2n1S(C)(=O)=O
Reaction #84219
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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