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OCCOCCO

CC(=O)O[C@H]1COC[C@H]1OC(=O)C(C)Cl
Reaction #3176
(±)-(3R,4S)-4-Acetoxy-3-(2-chloropropionyloxy)tetrahydrofuran
DOI: 10.6084/m9.figshare.5104873.v1
COCCOCCOCCOC(=O)C1CC1
Reaction #7072
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])C1OC1C(=O)[O-].[K+].[K+]
Reaction #8648
potassium epoxysuccinate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(O)C(O)C(=O)O
Reaction #54862
racemic acid
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
Выход 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
Выход 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
O=C(O)[C@H]1O[C@H]1C(=O)O
Reaction #82144
Cis-Epoxysuccinic Acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COCC2(COCc3ccc(OC)cc3)OC(=O)[C@H](OCc3ccccc3)[C@@H](OCc3ccccc3)[C@@H]2OCc2ccccc2)cc1
Reaction #87466
(3R,4S,5S)-3,4,5-tris-benzyloxy-6,6-bis-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-2-one
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COCC2(COCc3ccc(OC)cc3)OC(=O)[C@H](OCc3ccccc3)[C@@H](OCc3ccccc3)[C@@H]2OCc2ccccc2)cc1
Reaction #87486
(3R,4S,5S)-3,4,5-tris-benzyloxy-6,6-bis-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-2-one
Выход 72.0%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
Выход 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
Выход 23.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1C(O)CC(O)(C(=O)OCc2ccccc2)OC1C(O)C(O)COC(=O)C(NC(=O)OCc1ccccc1)C(C)C
Reaction #164435
( 1-5 )
Выход 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1C(COCc2ccccc2)OC(OC(=N)C(Cl)(Cl)Cl)C(OC(C)=O)C1OC(C)=O
Reaction #179800
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
OCCCCCCCCCCCCCCCCOC1OC(COCc2ccccc2)C(OCc2ccccc2)C(OCc2ccccc2)C1OCc1ccccc1
Reaction #192030
DOI: 10.1039/C8SC04228D
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