بحث البنية الفرعية

C1CCOC(C1)OCCCCl

COc1cc2c(cc1OCCCOC1CCCCO1)CCC2=O
Reaction #287079
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NCCCOC1CCCCO1
Reaction #298743
DOI: 10.1039/C8SC04228D
OCC(CCl)OC1CCCCO1
Reaction #320240
1-hydroxy-2-(tetrahydropyran-2-yl)oxy-3-chloropropane
DOI: 10.6084/m9.figshare.5104873.v1
CCCOC(=O)CCCCCCC1C(Cl)CC(OC2CCCCO2)C1C=O
Reaction #403269
DOI: 10.1039/C8SC04228D
CC(C)=CCC(C)[C@H](O)/C=C/[C@@H]1[C@@H](C/C=C\CCCC(=O)O)[C@H](Cl)C[C@H]1O
Reaction #413363
title compound
المردود 14.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC/C=C\C[C@@H]1[C@@H](/C=C/[C@@H](OC2CCCCO2)C(C)CC=C(C)C)[C@H](OC2CCCCO2)C[C@H]1Cl
Reaction #413364
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCC(C)[C@H](O)/C=C/[C@@H]1[C@@H](C/C=C\CCCC(=O)O)[C@@H](Cl)C[C@H]1O
Reaction #413365
carboxylic acid
المردود 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCC(C)[C@H](O)/C=C/[C@@H]1[C@@H](CCCCCCC(=O)O)[C@H](Cl)C[C@H]1O
Reaction #413366
carboxylic acid
المردود 43.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCC(C)[C@H](O)/C=C/[C@@H]1[C@@H](CCCCCCC(=O)NS(C)(=O)=O)[C@H](Cl)C[C@H]1O
Reaction #413368
title compound
المردود 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCC(C)[C@H](O)/C=C/[C@@H]1[C@@H](C/C=C\CCCC(=O)NS(C)(=O)=O)[C@H](Cl)C[C@H]1O
Reaction #413369
desired compound
المردود 53.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCC(C)(C)[C@H](O)/C=C/[C@@H]1[C@@H](C/C=C\CCCC(=O)O)[C@H](Cl)C[C@H]1O
Reaction #413370
title compound
المردود 51.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC/C=C\C[C@@H]1[C@@H](/C=C/[C@@H](OC2CCCCO2)C(C)(C)CC=C(C)C)[C@H](OC2CCCCO2)C[C@H]1Cl
Reaction #413371
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC(=O)CCCCCC[C@@H]1[C@@H](/C=C/[C@@H](O)CCC=C(C)C)[C@H](O)C[C@H]1Cl
Reaction #413372
title compound
المردود 59.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCC[C@@H]1[C@@H](/C=C/[C@H](CCC=C(C)C)OC2CCCCO2)[C@H](OC2CCCCO2)C[C@H]1Cl
Reaction #413373
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C/C(Cl)=C/CC(C)[C@H](O)/C=C/[C@@H]1[C@@H](C/C=C\CCCC(=O)O)[C@H](Cl)C[C@H]1O
Reaction #413374
title compound
المردود 59.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC/C=C\C[C@@H]1[C@@H](/C=C/[C@@H](OC2CCCCO2)C(C)C/C=C(/C)Cl)[C@H](OC2CCCCO2)C[C@H]1Cl
Reaction #413375
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C[O-]
Reaction #503692
formate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C)(C)[C@H](O)/C=C/[C@@H]1[C@@H](CC/C=C\CCC(=O)OC)[C@H](Cl)C[C@H]1O
Reaction #529970
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OCCCOC1CCCCO1)CCC2=O
Reaction #547527
6-Methoxy-5-[3-(tetrahydro-pyran-2-yloxy)-propoxy]-indan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(O[Si](C)(C)C(C)(C)C)C(=O)/C=C/[C@@H]1[C@@H](CCCc2ccc(C(=O)OC)s2)[C@H](Cl)C[C@H]1OC1CCCCO1
Reaction #716117
Compound 15
المردود 86.0%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي