Поиск подструктуры

657247

CCOC(=O)[C@@]1(N)CC(=O)NC1=O.Cl
Reaction #86028
title compound
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(N)CC(=O)NC1=O.Cl
Reaction #86033
title compound
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(n2cc(Cl)cc2C(=O)C(Cl)(Cl)Cl)CC(=O)NC1=O
Reaction #343778
title compound
Выход 41.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(n2cc(Br)cc2C(=O)C(Cl)(Cl)Cl)CC(=O)NC1=O
Reaction #343779
title compound
Выход 36.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(N)CC(=O)NC1=O.Cl
Reaction #558534
title compound
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(N)CC(=O)NC1=O.Cl
Reaction #558539
title compound
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NN)CC(=O)NC1=O.Cl
Reaction #644656
desired product
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(n2cccc2C(=O)C(Cl)(Cl)Cl)CC(=O)NC1=O
Reaction #644657
ethyl (R)-2,5-dioxo-3-(2-trichloroacetylpyrrol-1-yl)pyrrolidine-3-carboxylate
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NN)CC(=O)NC1=O.Cl
Reaction #1763115
desired product
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NN)CC(=O)NC1=O.Cl
Reaction #2030190
desired product
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NN)CC(=O)NC1=O.Cl
Reaction #2051360
desired product
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(n2cccc2C(=O)C(Cl)(Cl)Cl)CC(=O)NC1=O
Reaction #2051361
ethyl (R)-2,5-dioxo-3-(2-trichloroacetylpyrrol-1-yl)pyrrolidine-3-carboxylate
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1