Поиск подструктуры

36231

ClCC1OCOC1CCl
Reaction #5248
4,5-Dichloromethyl-1,3-dioxolane
Выход 89.5%DOI: 10.6084/m9.figshare.5104873.v1
COC1(OC)C2(Cl)CN(Cc3ccccc3)CC1(Cl)C(Cl)=C2Cl
Reaction #280115
DOI: 10.1039/C8SC04228D
ClCC1OCOC1CCl
Reaction #302645
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2C(=O)N1C(CCl)C(O)CCl
Reaction #1287989
DOI: 10.1039/C8SC04228D
COC1(OC)C2(Cl)C(Cl)=C(Cl)C1(Cl)C1OC(=O)OC12
Reaction #1382672
solid
Выход 94.5%DOI: 10.6084/m9.figshare.5104873.v1
COC1(OC)C2(Cl)C(Cl)=C(Cl)C1(Cl)C(O)C2O
Reaction #1382673
solid
Выход 78.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC3(Cl)C(Cl)=C(Cl)C(Cl)(C2)C3(OC)OC)cc1
Reaction #1382677
title compound
Выход 82.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1[C@@H](CCl)[C@H](O)CCl
Reaction #1455939
N-(1,4-Dichloro-2(S)-hydroxy-3(R)-butyl)phthalimide
Выход 104.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC3(Cl)C(Cl)=C(Cl)C(Cl)(C2)C3(OC)OC)cc1
Reaction #1650997
DOI: 10.1039/C8SC04228D
ClCC1OCOC1CCl
Reaction #2027414
4,5-Dichloromethyl-1,3-dioxolane
Выход 89.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C1OC(CCl)C(CCl)O1
Reaction #2027415
2-Isopropyl-4,5-dichloromethyl-1,3-dioxolane
DOI: 10.6084/m9.figshare.5104873.v1
COC1(OC)C2(Cl)C(Cl)=C(Cl)C1(Cl)C(O)C2O
Reaction #2398393
DOI: 10.1039/C8SC04228D