بحث البنية الفرعية

COCCOCCOC

COCCOCCOCCOC(=O)C1CC1
Reaction #7072
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(NCC(c4ccccc4)c4ccccc4)nc(C(=O)OC)nc32)[C@H](O)[C@@H]1O
Reaction #10537
title compound
المردود 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(NCC(c2ccccc2)c2ccccc2)c2ncn([C@@H]3O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)c2n1
Reaction #10563
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(NCC(c2ccccc2)c2ccccc2)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2n1
Reaction #10564
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCOCCOCc1cc(C(=O)NC2CCN(C(C)C)CC2)nn1CC(=O)Nc1ccc(Cl)cn1
Reaction #61546
1-[(5-Chloro-pyridin-2-ylcarbamoyl)-methyl]-5-[2-(2-methoxy-ethoxy)-ethoxymethyl]-1H-pyrazole-3-carboxylic acid (1-isopropyl-piperidin-4-yl)-amide
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
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
—
Reaction #92022
solid
المردود 53.0%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
COCOCCc1ccc(Cc2ccc(OC)cc2OC2OC(COC(C)=O)C(OC(C)=O)C(OC(C)=O)C2OC(C)=O)cc1
Reaction #182418
DOI: 10.1039/C8SC04228D
CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCOCCN=[N+]=[N-])c2)C1
Reaction #190620
DOI: 10.1039/C8SC04228D
OCC1OC(OCCc2c[nH]c3ccccc23)C(OCc2ccccc2)C(OCc2ccccc2)C1OCc1ccccc1
Reaction #195720
DOI: 10.1039/C8SC04228D
COCCOCCOCCOCC(=O)NN
Reaction #199908
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCOCC(COC1OC(CO)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O)OCCCCCCCCCCCCCC
Reaction #200148
DOI: 10.1039/C8SC04228D
CCOc1ccc(Cc2cc(C34OCC(CO)(O3)C(OCc3ccccc3)C(OCc3ccccc3)C4OCc3ccccc3)ccc2Cl)cc1F
Reaction #207583
DOI: 10.1039/C8SC04228D
الصفحة 1التالي