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997539

COCC1CC(C(=O)OC)N(C(=O)OC(C)(C)C)C1
Reaction #159165
title compound
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC1CC(C(=O)OCC(=O)c2ccc(Br)cc2)N(C(=O)OC(C)(C)C)C1
Reaction #159166
title compound
Ausbeute 97.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(COC(F)F)CN1C(=O)OC(C)(C)C
Reaction #159169
title compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(COC(F)F)CC1C(=O)OCC(=O)c1ccc(Br)cc1
Reaction #159170
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC1CC(C(=O)OC)N(C(=O)OC(C)(C)C)C1
Reaction #167108
title compound
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC1CC(C(=O)OCC(=O)c2ccc(Br)cc2)N(C(=O)OC(C)(C)C)C1
Reaction #167109
title compound
Ausbeute 97.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(COC(F)F)CN1C(=O)OC(C)(C)C
Reaction #167112
title compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(COC(F)F)CC1C(=O)OCC(=O)c1ccc(Br)cc1
Reaction #167113
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(COC(F)F)CN1C(=O)OC(C)(C)C
Reaction #221551
DOI: 10.1039/C8SC04228D
COCC1CC(C(=O)OC2CCc3cc4c(cc3C2=O)OCc2cc(C(=O)COC(=O)C3CCC(C)N3C(=O)OC(C)(C)C)ccc2-4)N(C(=O)OC(C)(C)C)C1
Reaction #301575
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC(COC(F)F)CC1C(=O)O
Reaction #404788
DOI: 10.1039/C8SC04228D
COCC1CC(C(=O)OC)N(C(=O)OC(C)(C)C)C1
Reaction #406332
DOI: 10.1039/C8SC04228D
COCC1CC(C(=O)OC)N(C(=O)OC(C)(C)C)C1
Reaction #504858
title compound
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC1CC(C(=O)OCC(=O)c2ccc(Br)cc2)N(C(=O)OC(C)(C)C)C1
Reaction #504859
title compound
Ausbeute 97.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(COC(F)F)CN1C(=O)OC(C)(C)C
Reaction #504862
title compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(COC(F)F)CC1C(=O)OCC(=O)c1ccc(Br)cc1
Reaction #504863
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C[C@@H](C(=O)OC)N(C(=O)OC(C)(C)C)C1
Reaction #677841
(2S,4S)-1-tert-butyl 2,4-dimethyl pyrrolidine-1,2,4-tricarboxylate
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H]1C[C@@H](C(=O)OC)N(C(=O)OC(C)(C)C)C1
Reaction #677843
(2S,4S)-1-tert-butyl 2-methyl 4-(methoxymethyl)pyrrolidine-1,2-dicarboxylate
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H]1C[C@@H](C(=O)O)N(C(=O)OC(C)(C)C)C1
Reaction #677844
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic acid
Ausbeute 100.2%DOI: 10.6084/m9.figshare.5104873.v1
COCC1CC(C(=O)OC)N(C(=O)OC(C)(C)C)C1
Reaction #789619
DOI: 10.1039/C8SC04228D
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