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342259

CC1CCNC(C(=O)OCc2ccccc2)C1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #94595
benzyl 4-methyl-2-piperidinecarboxylate p-toluenesulfonate
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OC(C)C(=O)N2C(C(=O)OCc3ccccc3)CC3CCCCC32)cc1
Reaction #264387
DOI: 10.1039/C8SC04228D
CCC[C@H](N[C@@H](C)C(=O)N1[C@@H](C(=O)OCc2ccccc2)C[C@@H]2CCCC[C@@H]21)C(=O)OCC
Reaction #360658
perindopril benzyl ester
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](N)C(=O)OCc1ccccc1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #583946
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)[C@@H](N)Cc1ccc(OC(C)(C)C)cc1)C(=O)OCc1ccccc1
Reaction #610537
H-Tyr(tBu)-Leu-OBzl
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](N)C(=O)OCc1ccccc1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #701947
leucine benzyl ester p-toluene sulfonate
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](N)C(=O)OCc1ccccc1
Reaction #701948
benzyl leucinate
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCNC(C(=O)OCc2ccccc2)C1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #703590
benzyl 4-methyl-2-piperidinecarboxylate p-toluenesulfonate
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@H](CCCNC(=N)N[N+](=O)[O-])NC(=O)CCNC(=O)OCc1ccccc1)C(=O)OCc1ccccc1
Reaction #703667
Z-β-Ala-Arg(NO2)-Gly-Phe-Phe-Tyr-Leu-OBzl
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCNC(C(=O)OCc2ccccc2)C1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #926147
benzyl 4-methyl-2-piperidinecarboxylate p-toluenesulfonate
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCNC(C(=O)OCc2ccccc2)C1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #927043
benzyl 4-methyl-2-piperidinecarboxylate p-toluenesulfonate
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCNC(C(=O)OCc2ccccc2)C1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #954087
benzyl 4-methyl-2-piperidinecarboxylate p-toluenesulfonate
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O[C@H](C)C(=O)N2[C@H](C(=O)OCc3ccccc3)C[C@@H]3CCCC[C@@H]32)cc1
Reaction #987578
benzyl (2S,3aS,7aS)-1-[(2R)-2-{p-toluenesulphonyloxy}propionyl]octahydro-1H-indole-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](N)C(=O)OCc1ccccc1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #989402
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)N2CCSC[C@H]2C(=O)NC(CC(C)C)C(=O)OCc2ccccc2)cc1
Reaction #1055703
product
Ausbeute 95.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](N)C(=O)OCc1ccccc1
Reaction #1177006
colorless solid
Ausbeute 67.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)OC(C)(C)C)C(=O)N1[C@H](C(=O)OCc2ccccc2)C[C@@H]2CCCC[C@@H]21
Reaction #1269570
Benzyl (2S,3aS,7aS)-1-{(2S)-2-[(tert-butyloxycarbonyl)-amino]-propionyl}-octahydro-1H-indole-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](N)C(=O)OCc1ccccc1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #1359718
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](N)C(=O)OCc1ccccc1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #1363162
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@H](CCCNC(=N)N[N+](=O)[O-])NC(=O)CCNC(=O)OCc1ccccc1)C(=O)OCc1ccccc1
Reaction #1501867
Z-β-Ala-Arg(NO2)-Gly-Phe-Phe-Tyr-Leu-OBzl
DOI: 10.6084/m9.figshare.5104873.v1
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