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CC(C)(C)OC(=O)[C@@H]1C[C@@H](OS(C)(=O)=O)CN1C(=O)OC(C)(C)C
Reaction #486696
(4R)-1-(tert-Butyloxycarbonyl)-4-(methanesulfonyloxy)-L-Proline tert-Butyl Ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1C[C@H](C#N)CN1C(=O)OC(C)(C)C
Reaction #486697
desired title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1C[C@@H](C#N)CN1C(=O)OC(C)(C)C
Reaction #486700
desired title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1C[C@H](OC(=O)c2ccc([N+](=O)[O-])cc2)CN1C(=O)OC(C)(C)C
Reaction #486706
desired product
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1C[C@H](O)CN1C(=O)OC(C)(C)C
Reaction #486707
title compound
Rendimiento 82.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1C[C@H](OS(C)(=O)=O)CN1C(=O)OC(C)(C)C
Reaction #486708
(4S)-1-(tert-Butyloxycarbonyl)-4-(methanesulfonyloxy)-L-Proline tert-Butyl Ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1C[C@@H](N=[N+]=[N-])CN1C(=O)OC(C)(C)C
Reaction #486709
azide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OC2CC(C(=O)OC(C)(C)C)N(C(=O)OC(C)(C)C)C2)cc1
Reaction #634756
Di-tert-butyl 4-(tosyloxy)pyrrolidine-1,2-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1CC(O)CN1C(=O)OC(C)(C)C
Reaction #907693
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C1CC(Oc2ccc3ccncc3c2)CN1C(=O)OC(C)(C)C
Reaction #1212534
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C1CC(O)CN1C(=O)OC(C)(C)C
Reaction #1287750
DOI: 10.1039/C8SC04228D
Cc1ccc(S(=O)(=O)O[C@@H]2C[C@@H](C(=O)OC(C)(C)C)N(C(=O)OC(C)(C)C)C2)cc1
Reaction #1530139
title compound
Rendimiento 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1C[C@H](Oc2ccc3ccncc3c2)CN1C(=O)OC(C)(C)C
Reaction #1530145
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1(O)CC(C(=O)OC(C)(C)C)N(C(=O)OC(C)(C)C)C1
Reaction #1631062
DOI: 10.1039/C8SC04228D
CCOC(=O)CC1(O)C[C@@H](C(=O)OC(C)(C)C)N(C(=O)OC(C)(C)C)C1
Reaction #2125735
(2S)-di-tert-butyl 4-(2-ethoxy-2-oxoethyl)-4-hydroxypyrrolidine-1,2-dicarboxylate
Rendimiento 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CC2(CNC(=O)O2)CN1C(=O)OC(C)(C)C
Reaction #2125736
(8S)-di-tert-butyl 2-oxo-1-oxa-3,7-diazaspiro[4.4]nonane-7,8-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1C[C@@]2(CN(c3cccc(Cl)c3)C(=O)O2)CN1C(=O)OC(C)(C)C
Reaction #2125743
(5S,8S)-di-tert-butyl 3-(3-chlorophenyl)-2-oxo-1-oxa-3,7-diazaspiro[4.4]nonane-7,8-dicarboxylate
Rendimiento 36.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@]2(CN1)CN(c1cccc(Cl)c1)C(=O)O2
Reaction #2125744
(5S,8S)-methyl-3-(3-chlorophenyl)-2-oxo-1-oxa-3,7-diazaspiro[4.4]nonane-8-carboxylate
Rendimiento 81.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1C[C@]2(CN(c3cccc(Cl)c3)C(=O)O2)CN1C(=O)OC(C)(C)C
Reaction #2125748
(5R,8S)-di-tert-butyl 3-(3-chlorophenyl)-2-oxo-1-oxa-3,7-diazaspiro[4.4]nonane-7,8-dicarboxylate
Rendimiento 21.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1C[C@@]2(CN(c3cccc(Cl)c3)C(=O)O2)CN1C(=O)OC(C)(C)C
Reaction #2125751
(5S,8S)-di-tert-butyl 3-(3-chlorophenyl)-2-oxo-1-oxa-3,7-diazaspiro[4.4]nonane-7,8-dicarboxylate
Rendimiento 19.3%DOI: 10.6084/m9.figshare.5104873.v1
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