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1079896

CCN(C(=O)OC(C)(C)C)[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](CCSC)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)NCCCCCC(=O)OC.CCN(C(=O)OC(C)(C)C)[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](CCSC)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)NCCCCCC(=O)OC.Cl.Cl.O
Reaction #3884
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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 #8956
L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC2(CC(CC)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #44022
mixture
収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC2(CC(CO)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #44023
mixture
収率 57.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CC[C@H](CN)CC1.Cl
Reaction #44975
methyl trans-4-(aminomethyl)-cyclohexanecarboxylate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCNC(=O)C(F)(F)F
Reaction #47713
product ( 3 )
収率 87.0%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 #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
COC(=O)C1CCC(CNC(=O)c2cccc(CS(=O)(=O)C=C3CN(C(c4ccc(Cl)cc4)c4ccc(Cl)cc4)C3)c2)CC1
Reaction #53500
4-{[3-({1-[bis-(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)benzoylamino]methyl}cyclohexanecarboxylic acid methyl ester
収率 38.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCNS(=O)(=O)c1cccc2ccccc12
Reaction #78885
6(1-naphthalenesulfonyl)aminocaproic acid methyl ester
収率 54.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1NCCCC1C.Cl
Reaction #89119
methyl 3-methylpiperidine-2-carboxylate hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N1CCC(Oc2cc3c(Nc4ccc(F)c(Cl)c4F)ncnc3cc2OC)CC1C(=O)O
Reaction #182329
DOI: 10.1039/C8SC04228D
Cc1cc(Cl)ccc1NC(=O)CC(CCC(=O)O)c1noc(C2CC(CC(C)(C)C)C2)c1C1CC1
Reaction #196778
DOI: 10.1039/C8SC04228D
O=CC(CCCCNS(=O)(=O)c1ccc(Cl)cc1)CCCc1cccnc1
Reaction #200654
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=C(NCc2ccc(Cl)cc2)CCC1
Reaction #212099
DOI: 10.1039/C8SC04228D
CCOC(=O)C1C2CCC(C2)C1NCc1ccc(F)c(Cl)c1
Reaction #213510
DOI: 10.1039/C8SC04228D
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