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1020811

COc1cc(C=O)ccc1C(=O)CNCCN1CCC(OC(=O)Nc2ccccc2-c2ccccc2)CC1
Reaction #42143
Biphenyl-2-ylcarbamic acid 1-{2-[(4-formyl-2-methoxybenzoyl)methylamino]ethyl}piperidin-4-yl Ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC(c3cccc(F)c3F)=CC[C@@H](NC(=O)OCc3ccccc3)C2=O)c(OC)c1
Reaction #42664
title compound
収率 57.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC=C(c2cccc(F)c2F)CNC1=O)OCc1ccccc1
Reaction #42665
title compound
収率 66.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC(c3cccc(F)c3F)=CC[C@@H](NC(=O)OCc3ccccc3)C2=O)c(OC)c1
Reaction #48408
title compound
収率 57.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC=C(c2cccc(F)c2F)CNC1=O)OCc1ccccc1
Reaction #48409
title compound
収率 66.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N2CCN(C(=O)C[C@@H](OC(=O)NCCc3ccccc3)c3ccccc3)CC2)cc1OC
Reaction #72490
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(NC(=O)OCc1ccccc1)C1(c2ccc(OC)cc2)CCC(=O)CC1
Reaction #73473
ketone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)CN)C(=O)N[C@@H](Cc1ccccc1)C(O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CN)C(C)C
Reaction #81108
desired compound
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)C(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(N)=O
Reaction #93624
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #93651
B7
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)C(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(N)=O
Reaction #93655
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(c2ccc(F)c(-c3nc4cc(OC)ccc4n3C(=O)OC(C)(C)C)c2)CC1
Reaction #164264
title compound
収率 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)C(Cc1ccc2ccccc2c1)N(C)C(=O)C=CCC(C)(C)NC(=O)OC(C)(C)C)C(CNC(=S)NC1CC1)Cc1ccccc1
Reaction #186924
DOI: 10.1039/C8SC04228D
CC(C)C(CCNC(=N)N)CC(O)C(CC1CCCCC1)NC(=O)C(Cc1c[nH]cn1)NC(=O)C(Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #188495
DOI: 10.1039/C8SC04228D
CC(C)(C)N1C(=O)CC(c2ccc(CC(NC(=O)OCc3ccccc3)C(N)=O)cc2)S1(=O)=O
Reaction #200412
DOI: 10.1039/C8SC04228D
CCN(C(=O)OC1CCCCC1)c1ccc(Oc2ncnc3cc(OC)c(OC)cc23)cc1Cl
Reaction #201490
DOI: 10.1039/C8SC04228D
N#Cc1cc2c(Oc3ccc(NC(=O)Nc4nccs4)c(F)c3)ccnc2cc1OCc1ccccc1
Reaction #203866
DOI: 10.1039/C8SC04228D
CN(C(=O)C(Cc1ccc2ccccc2c1)N(C)C(=O)C=CCC(C)(C)NC(=O)OC(C)(C)C)C(CNC(=S)NC1CC1)Cc1ccccc1
Reaction #204968
DOI: 10.1039/C8SC04228D
Nc1ccc(C2=NC(Cc3ccccc3Br)C(=O)Nc3ccc(Cl)cc32)cc1
Reaction #213057
DOI: 10.1039/C8SC04228D
COc1cccc(C(=O)N[C@@H](CC2CCCCC2)C(=O)N[C@@H](COCc2ccccc2)CN2CCc3cc(F)ccc32)c1
Reaction #219324
title material
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
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