Поиск подструктуры

1335869

CCCCC/C=C\C/C=C\C/C=C\CCCCC(=O)OCCCOC(=O)c1cc(I)cc(I)c1I
Reaction #56581
1-(2,3,5-triiodobenzoyloxy)-3-(z,z,z-octadeca-6,9,12-trienoyloxy)propane
DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(I)c(C(=O)NCC(O)CO)c(I)c(C(=O)NC(CO)CO)c1I
Reaction #70113
5-amino-N1-(1,3-dihydroxypropan-2-yl)-N3-(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamide
Выход 57.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCNC(=O)c1ccccc1I
Reaction #77489
2-iodo-benzoic acid allylamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1ccc(Cl)c(I)c1C(=O)c1ccccc1
Reaction #165575
chloro-iododibenzoylbenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCC(NC(=O)c1c(I)c(NC(C)=O)c(I)c(NC(C)=O)c1I)C(=O)OCC
Reaction #180829
DOI: 10.1039/C8SC04228D
O=C(Cl)c1ccc(Cl)cc1I
Reaction #184233
DOI: 10.1039/C8SC04228D
C=CCN(CC=C)C(=O)c1c(I)c(NC(=O)COC(C)=O)c(I)c(C(=O)Cl)c1I
Reaction #189791
DOI: 10.1039/C8SC04228D
CC(=O)OCC(=O)N(C)c1c(I)c(C(=O)Cl)c(I)c(C(=O)Cl)c1I
Reaction #191769
DOI: 10.1039/C8SC04228D
CNC(=O)c1c(I)c(N)c(I)c(C(=O)Cl)c1I
Reaction #197886
DOI: 10.1039/C8SC04228D
O=C(Cl)c1ccccc1I
Reaction #226423
DOI: 10.1039/C8SC04228D
O=C(Cl)c1ccccc1
Reaction #228162
DOI: 10.1039/C8SC04228D
O=C1C(=O)c2ccccc2C2=C1SCC1(CCN(C(=O)c3ccccc3I)CC1)O2
Reaction #228378
DOI: 10.1039/C8SC04228D
CNC(=O)c1c(I)c(NC(=O)COC)c(I)c(C(=O)Cl)c1I
Reaction #242536
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCCNC(=O)c1ccccc1I
Reaction #248717
DOI: 10.1039/C8SC04228D
CCCCCCNC(=O)c1ccccc1I
Reaction #251235
DOI: 10.1039/C8SC04228D
CCOC(=O)CC(NC(=O)c1c(I)c(NC(C)=O)c(I)c(NC(C)=O)c1I)C(=O)OCC
Reaction #258755
DOI: 10.1039/C8SC04228D
OC(=S)c1ccccc1I
Reaction #260344
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCCOC(=O)c1ccccc1I
Reaction #263228
DOI: 10.1039/C8SC04228D
C=CCNC(=O)c1c(I)c(NC(=O)COC(C)=O)c(I)c(C(=O)Cl)c1I
Reaction #263419
DOI: 10.1039/C8SC04228D
O=C(NCc1ccccc1)c1ccccc1I
Reaction #267198
DOI: 10.1039/C8SC04228D
Страница 1Далее