子结构搜索

828092

CCCCOC(=O)N(C)Cc1ccccc1CC(=O)NC1C(=O)N2C(C(=O)O)=C(CSc3ccc4nn(CCC(=O)O)c(=O)n4n3)CS[C@H]12
Reaction #55280
title compound
收率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C(CO)CN(C(=O)OC(C)(C)C)C2
Reaction #376642
DOI: 10.1039/C8SC04228D
C=C(C(=O)OCC)c1ccc(NC(=O)OC(C)(C)C)cc1CN(C)C(=O)OC(C)(C)C
Reaction #796034
15E
收率 31.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(c2ccc(NC(=O)OC(C)(C)C)cc2CN(C)C(=O)OC(C)(C)C)CC1
Reaction #796035
15F
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(c2ccc(N)cc2CNC)CC1.Cl
Reaction #796036
15G
收率 111.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C(CO)CN(C(=O)OC(C)(C)C)C2
Reaction #1437259
tert-Butyl 4-(hydroxymethyl)-6-methoxy-3,4-dihydro-2(1H)-isoquinoline-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)N(C)Cc1ccccc1CC(=O)NC1C(=O)N2C(C(=O)O)=C(CSc3ccc4nn(CCC(=O)O)c(=O)n4n3)CS[C@H]12
Reaction #2137045
title compound
收率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)N(C)Cc1ccccc1CC(=O)NC1C(=O)N2C(C(=O)O)=C(CSc3ccc4nn(CCC(=O)O)c(=O)n4n3)CS[C@H]12
Reaction #2170090
title compound
收率 50.0%DOI: 10.6084/m9.figshare.5104873.v1