部分構造検索

13190

NCCCC[C@H](N)C(=O)O
Reaction #8947
L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@H](N)C(=O)O
Reaction #8949
L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@H](N)C(=O)O
Reaction #8952
L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@H](N)C(=O)O
Reaction #8954
L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@H](N)C(=O)O
Reaction #8955
L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@H](N)C(=O)O
Reaction #8956
L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CCC(CN)c1cccc(Cl)c1Cl)C(=O)OCc1ccccc1
Reaction #48399
title compound
収率 182.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@@H]1CCC(c2cccc(Cl)c2Cl)CNC1=O
Reaction #48400
di-tert-butyl [(3R)-6-(2,3-dichlorophenyl)-2-oxoazepan-3-yl]imidodicarbonate
収率 82.3%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N[C@@H](CCCCNC(=O)OCc1ccccc1)C(=O)Oc1cccc2ccccc12
Reaction #215021
Nε -benzyloxycarbonyl-L-lysine 1-naphthyl ester hydrochloride
収率 209.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(F)[C@@H]2C[C@@H](NCc3ccc(Cl)c(Cl)c3)[C@@](NC(=O)OC(C)(C)C)(C(=O)OCC)[C@@H]21
Reaction #217691
(1R,2R,3R,5R,6R)-2-t-butoxycarbonylamino-3-(3,4-dichlorobenzylamino)-6-fluoro-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester
収率 39.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(N)[C@H]2[C@@H](C[C@H]1NCc1ccc(Cl)c(Cl)c1)[C@]2(F)C(=O)OCC
Reaction #217692
(1R,2R,3R,5R,6R)-2-amino-3-(3,4-dichlorobenzylamino)-6-fluoro-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester
収率 92.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(F)[C@@H]2C[C@@H](NC(=O)c3ccc(Cl)c(Cl)c3)[C@@](NC(=O)OC(C)(C)C)(C(=O)OCC)[C@@H]21
Reaction #217693
(1R,2R,3R,5R,6R)-2-t-butoxycarbonylamino-3-(3,4-dichlorobenzoylamino)-6-fluoro-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester
収率 84.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](N)CCCCN.ClCCCl
Reaction #347679
EDC LME
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H](N)CCCCN.Cl.Cl
Reaction #349964
lysine ethyl ester dihydrochloride
収率 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CCC(CN)c1cccc(Cl)c1Cl)C(=O)OCc1ccccc1
Reaction #359097
title compound
収率 182.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@@H]1CCC(c2cccc(Cl)c2Cl)CNC1=O
Reaction #359098
di-tert-butyl [(3R)-6-(2,3-dichlorophenyl)-2-oxoazepan-3-yl]imidodicarbonate
収率 82.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(F)C2CC(NC(=O)c3ccc(Cl)c(Cl)c3)C(NC(=O)OC(C)(C)C)(C(=O)OCC)C21
Reaction #400455
DOI: 10.1039/C8SC04228D
COC(=O)C(CCCCNC(=O)COCc1ccccc1)NC(=O)COCc1ccccc1
Reaction #470381
2
収率 31.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](N)CCCCN.ClCCCl
Reaction #484481
EDC LME
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CCCCNC(=O)COCc1ccccc1)NC(=O)COCc1ccccc1
Reaction #493973
2
収率 31.8%DOI: 10.6084/m9.figshare.5104873.v1
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