112 件の反応に参加

9355

CC(C)(C)OC(=O)N1C[C@H](O)C[C@H]1C(N)=O
Reaction #5162
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)OC(C)(C)C
Reaction #5167
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CN(C)C(=O)[C@@H]1C[C@@H](O)CN1C(=O)OC(C)(C)C
Reaction #5173
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)OC(=O)N1C[C@H](OCc2cccc3ccccc23)C[C@H]1C(=O)O
Reaction #61358
title compound
収率 56.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(C)OC(=O)N1C[C@H](O)C[C@H]1C(=O)OC(c1ccccc1)c1ccccc1
Reaction #79470
N-tert-butoxycarbonyl-trans-4-hydroxy-L-proline diphenylmethyl ester
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C[N-]C.Cl.O=C(O)[C@@H]1C[C@@H](O)CN1
Reaction #314407
L-trans-4-Hydroxyproline N,N-dimethylamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC(C)(C)OC(=O)N1C[C@H](Oc2nc3ccccc3nc2-c2nc3ccccc3s2)C[C@H]1C(=O)O
Reaction #325258
(2S,4R)-1-(tert-butoxycarbonyl)-4-(3-(benzo[d]thiazol-2-yl)quinoxalin-2-yloxy)pyrrolidine-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)OC(=O)N1C[C@H](Oc2nc3ccccc3c3ccccc23)C[C@H]1C(=O)O
Reaction #325261
(2S,4R)-1-(tert-butoxycarbonyl)-4-(phenanthridin-6-yloxy)pyrrolidine-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
c1ccc2nccnc2c1
Reaction #327421
desired product 1-1
収率 283.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)OC(=O)N1C[C@H](O)C[C@H]1C(=O)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #363947
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
C[N-]C.Cl.O=C(O)[C@@H]1C[C@@H](O)CN1
Reaction #434838
L-trans-4-Hydroxyproline N,N-dimethylamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CC(C)(C)OC(=O)N1CC(=O)C[C@H]1C(=O)O
Reaction #474388
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CCOC(=O)[C@@H]1C[C@@H](Oc2nccc3cc(OC)c(Br)cc23)CN1.Cl
Reaction #476379
title compound
収率 70.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
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
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
C=C[C@@H]1C[C@]1(NC(=O)[C@@H]1C[C@@H](O)CN1C(=O)OC(C)(C)C)C(=O)OCC
Reaction #490593
(2S,4R)-tert-butyl 2-((1R,2S)-1-(ethoxycarbonyl)-2-vinylcyclopropylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
C=C[C@@H]1C[C@]1(NC(=O)[C@@H]1C[C@@H](O)CN1C(=O)OC(C)(C)C)C(=O)OCC
Reaction #490603
oil
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
COC(=O)[C@@H]1CC(=O)CN1C(=O)OC(C)(C)C
Reaction #512593
1-tert-butyl 2-methyl (2S)-4-oxopyrrolidine-1,2-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CC(C)(C)NC(=O)[C@@H]1C[C@@H](O)CN1C(=O)OC(C)(C)C
Reaction #514566
title compound
収率 189.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
CC(C)(C)OC(=O)N1C[C@H](OCc2cccc3ccccc23)C[C@H]1C(=O)O
Reaction #517637
title compound
収率 56.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
CC(C)(C)OC(=O)N1CC(=O)C[C@H]1C(=O)O
Reaction #545086
(2S)-1-(tert-butoxycarbonyl)-4-oxo-2-pyrrolidinecarboxylic acid
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
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