部分構造検索

556399

CCN1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #76503
9-Ethyl-1,4,7,8,9,10-hexahydro-6-nitro-pyrido[3,4-f]quinoxaline-2,3-dione
収率 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1.CS(=O)(=O)O
Reaction #76504
title compound
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C(=O)N2CCc3ccc4[nH]c(=O)c(=O)[nH]c4c3C2)CC1
Reaction #226483
DOI: 10.1039/C8SC04228D
O=C(C1CCNCC1)N1CCc2ccc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #242476
DOI: 10.1039/C8SC04228D
O=C(c1ccc(Cl)cc1)N1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #253034
DOI: 10.1039/C8SC04228D
O=c1[nH]c2cc(Br)c3c(c2[nH]c1=O)CN(Cc1ccccc1)CC3
Reaction #1193608
title compound
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Br)c3c(c2[nH]c1=O)CN(CCc1ccccc1)CC3
Reaction #1193611
title compound
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Br)c3c(c2[nH]c1=O)CN(CCCc1ccccc1)CC3
Reaction #1193614
title compound
収率 60.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C(=O)N2CCc3ccc4[nH]c(=O)c(=O)[nH]c4c3C2)CC1
Reaction #1193622
solid
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C1CCNCC1)N1CCc2ccc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #1193623
solid
収率 101.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Cl)cc1)N1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #1193624
solid
収率 104.4%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Br)c3c(c2[nH]c1=O)CN(CCc1ccccc1)CC3
Reaction #1618023
title compound
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Br)c3c(c2[nH]c1=O)CN(CCCc1ccccc1)CC3
Reaction #1618026
title compound
収率 60.3%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2ccc3c(c2[nH]c1=O)CN(Cc1ccc(C(F)(F)F)cc1)CC3
Reaction #1618029
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C(=O)N2CCc3ccc4[nH]c(=O)c(=O)[nH]c4c3C2)CC1
Reaction #1618036
solid
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C1CCNCC1)N1CCc2ccc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #1618037
solid
収率 101.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Cl)cc1)N1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #1618038
solid
収率 104.4%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CC(=O)N1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #1826856
solid
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)O
Reaction #2425678
DOI: 10.1039/C8SC04228D
CCN1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #2433584
DOI: 10.1039/C8SC04228D