部分構造検索

657986

CCOC(=O)[C@@]1(NC(=O)OC(C)(C)C)CC(=O)NC1=O
Reaction #86027
title compound
収率 88.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(N)CC(=O)NC1=O.Cl
Reaction #86028
title compound
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(NC(=O)OC(C)(C)C)CC(=O)NC1=O
Reaction #86032
title compound
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(N)CC(=O)NC1=O.Cl
Reaction #86033
title compound
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(N(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)CC(=O)NC1=O
Reaction #199581
DOI: 10.1039/C8SC04228D
CCOC(=O)[C@@]1(NC(=O)OC(C)(C)C)CC(=O)NC1=O
Reaction #558533
title compound
収率 88.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(N)CC(=O)NC1=O.Cl
Reaction #558534
title compound
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(NC(=O)OC(C)(C)C)CC(=O)NC1=O
Reaction #558538
title compound
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(N)CC(=O)NC1=O.Cl
Reaction #558539
title compound
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(N(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)CC(=O)NC1=O
Reaction #644655
ethyl 3-[N,N′-bis(tert-butyloxycarbonyl)hydrazino]-2,5-dioxopyrrolidine-3-carboxy late
収率 83.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NN)CC(=O)NC1=O.Cl
Reaction #644656
desired product
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(N(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)CC(=O)NC1=O
Reaction #1763114
desired product
収率 83.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NN)CC(=O)NC1=O.Cl
Reaction #1763115
desired product
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(N)CC(=O)NC1=O
Reaction #1763116
desired product
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(N(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)CC(=O)NC1=O
Reaction #2030189
desired product
収率 83.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NN)CC(=O)NC1=O.Cl
Reaction #2030190
desired product
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(N)CC(=O)NC1=O
Reaction #2030191
desired product
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(N(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)CC(=O)NC1=O
Reaction #2051359
ethyl 3-[N,N′-bis(tert-butyloxycarbonyl)hydrazino]-2,5-dioxopyrrolidine-3-carboxy late
収率 83.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NN)CC(=O)NC1=O.Cl
Reaction #2051360
desired product
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1