Recherche de Sous-structure

721114

CC(=O)N[C@@]1(C(=O)NC(C)(C)C)CN(C(=O)OC(C)(C)C)C[C@@H]1CCCB1OC(C)(C)C(C)(C)O1
Reaction #89633
(3R,4S)-tert-butyl 3-acetamido-3-(tert-butylcarbamoyl)-4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propyl)pyrrolidine-1-carboxylate
Rendement 82.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #89634
HCl
DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CNC[C@@H]1CCCB(O)O
Reaction #89635
(3R,4S)-3-amino-4-(3-boronopropyl)pyrrolidine-3-carboxylic acid
Rendement 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CN1C[C@H](CCCB(O)O)[C@](N)(C(=O)O)C1
Reaction #89636
(3R,4S)-3-amino-4-(3-boronopropyl)-1-isobutylpyrrolidine-3-carboxylic acid
Rendement 32.3%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CN(Cc2ccccc2)C[C@@H]1CCCB(O)O
Reaction #89637
(3R,4S)-3-amino-1-benzyl-4-(3-boronopropyl)pyrrolidine-3-carboxylic acid
Rendement 54.4%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CN(Cc2cccnc2)C[C@@H]1CCCB(O)O
Reaction #89638
(3R,4S)-3-amino-4-(3-boronopropyl)-1-(pyridin-3-ylmethyl)pyrrolidine-3-carboxylic acid
Rendement 84.5%DOI: 10.6084/m9.figshare.5104873.v1
NC1CCCC1N1C[C@H](CCCB(O)O)[C@](N)(C(=O)O)C1
Reaction #89639
(3R,4S)-3-amino-1-(2-aminocyclopentyl)-4-(3-boronopropyl)pyrrolidine-3-carboxylic acid
Rendement 77.5%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CN(CC2CCNCC2)C[C@@H]1CCCB(O)O
Reaction #89640
(3R,4S)-3-amino-4-(3-boronopropyl)-1-(piperidin-4-ylmethyl)pyrrolidine-3-carboxylic acid
Rendement 42.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CC(C)(C)CN1C[C@H](CCCB(O)O)[C@](N)(C(=O)O)C1
Reaction #89641
(3R,4S)-3-amino-4-(3-boronopropyl)-1-(3-(dimethylamino)-2,2-dimethylpropyl)pyrrolidine-3-carboxylic acid
Rendement 21.9%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CN(CC2CCCNC2)C[C@@H]1CCCB(O)O
Reaction #89642
(3R,4S)-3-amino-4-(3-boronopropyl)-1-(piperidin-3-ylmethyl)pyrrolidine-3-carboxylic acid
Rendement 39.6%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CN(Cc2ccnc3ccccc23)C[C@@H]1CCCB(O)O
Reaction #89643
(3R,4S)-3-amino-4-(3-boronopropyl)-1-(quinolin-4-ylmethyl)pyrrolidine-3-carboxylic acid
Rendement 27.4%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CN(Cc2c[nH]cn2)C[C@@H]1CCCB(O)O
Reaction #89644
(3R,4S)-1-((1H-imidazol-4-yl)methyl)-3-amino-4-(3-boronopropyl)pyrrolidine-3-carboxylic acid
Rendement 25.7%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CN(CC2CCCCN2)C[C@@H]1CCCB(O)O
Reaction #89645
(3R,4S)-3-amino-4-(3-boronopropyl)-1-(piperidin-2-ylmethyl)pyrrolidine-3-carboxylic acid
Rendement 99.6%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CN(CCCc2ccc(Cl)cc2)C[C@@H]1CCCB(O)O
Reaction #89646
(3R,4S)-3-amino-4-(3-boronopropyl)-1-(3-(4-chlorophenyl)propyl)pyrrolidine-3-carboxylic acid
Rendement 45.7%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CN(c2ncnc3nc[nH]c23)C[C@@H]1CCCB(O)O
Reaction #89647
(3R,4S)-3-amino-4-(3-boronopropyl)-1-(7H-purin-6-yl)pyrrolidine-3-carboxylic acid
Rendement 20.0%DOI: 10.6084/m9.figshare.5104873.v1
NCCN1C[C@H](CCCB(O)O)[C@](N)(C(=O)O)C1
Reaction #89648
(3R,4S)-3-amino-1-(2-aminoethyl)-4-(3-boronopropyl)pyrrolidine-3-carboxylic acid
Rendement 49.4%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CN(c2cncc(C(=O)O)c2)C[C@@H]1CCCB(O)O
Reaction #89649
5-((3R,4S)-3-amino-4-(3-boronopropyl)-3-carboxypyrrolidin-1-yl)nicotinic acid
Rendement 48.6%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CN(C2CCNCC2)C[C@@H]1CCCB(O)O
Reaction #89650
(3R,4S)-3-amino-4-(3-boronopropyl)-1-(piperidin-4-yl)pyrrolidine-3-carboxylic acid
Rendement 97.6%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CN(C2CCNC2)C[C@@H]1CCCB(O)O
Reaction #89651
(3R,4S)-3-amino-4-(3-boronopropyl)-1,3′-bipyrrolidine-3-carboxylic acid
Rendement 112.2%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CN(C2CCCNC2)C[C@@H]1CCCB(O)O
Reaction #89652
(3R,4S)-3-amino-4-(3-boronopropyl)-1-(piperidin-3-yl)pyrrolidine-3-carboxylic acid
Rendement 92.3%DOI: 10.6084/m9.figshare.5104873.v1
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