Teilstruktursuche

431613

CCOC(=O)[C@@]1(NC(=O)OC(C)(C)C)CC(=O)NC1=O
Reaction #86027
title compound
Ausbeute 88.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(N)CC(=O)NC1=O.Cl
Reaction #86028
title compound
Ausbeute 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
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(N)CC(=O)NC1=O.Cl
Reaction #86033
title compound
Ausbeute 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
CC(C)(C)OC(=O)NC12CNCC1CCOC2
Reaction #388828
DOI: 10.1039/C8SC04228D
COC(=O)C1(NC(=O)OC(C)(C)C)CCN(Cc2ccccc2)C1
Reaction #426198
methyl 1-benzyl-3-(tert-butoxycarbonylamino)pyrrolidine-3-carboxylate
Ausbeute 79.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1(CO)CCN(Cc2ccccc2)C1
Reaction #426199
tert-butyl 1-benzyl-3-(hydroxymethyl)pyrrolidin-3-ylcarbamate
Ausbeute 56.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@]1(CO)CCNC1
Reaction #426200
(R)-tert-butyl 3-(hydroxymethyl)pyrrolidin-3-ylcarbamate
Ausbeute 95.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(NC(=O)OC(C)(C)C)CC(=O)NC1=O
Reaction #558533
title compound
Ausbeute 88.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(N)CC(=O)NC1=O.Cl
Reaction #558534
title compound
Ausbeute 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
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(N)CC(=O)NC1=O.Cl
Reaction #558539
title compound
Ausbeute 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
Ausbeute 83.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NN)CC(=O)NC1=O.Cl
Reaction #644656
desired product
Ausbeute 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
Ausbeute 83.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NN)CC(=O)NC1=O.Cl
Reaction #1763115
desired product
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(N)CC(=O)NC1=O
Reaction #1763116
desired product
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1CS[C@H]2C[C@@](CO)(NC(=O)OC(C)(C)C)C(=O)N21
Reaction #1830439
Methyl (3R,6S,7aS)-6-tert-butoxycarbonylamino-6-hydroxymethyl-5-oxohexahydropyrrolo[2,1-b]thiazole-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@]12CNC[C@H]1CCOC2
Reaction #2004576
title compound
Ausbeute 98.7%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter