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637714

O=c1[nH]cnc2sc3c(c12)CCC3
Reaction #51063
3,5,6,7-Tetrahydro-4H-cyclopenta[4,5]thieno[2,3-d]pyrimidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCN(C(=O)C(C)C)c1sc(CC)cc1C(=O)OCC
Reaction #55940
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCc2sc3nc[nH]c(=O)c3c2C1
Reaction #66837
title compound
収率 56.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)c2cccc(O)c2)sc(N=Nc2nc(N)c(O)cc2Br)c1C(=O)OC(C)(C)C
Reaction #95994
red solid
収率 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(CC)sc1Nc1ccccc1[N+](=O)[O-]
Reaction #174815
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)c1c(N)sc2c1CCOC2CN
Reaction #175907
DOI: 10.1039/C8SC04228D
CC(C)CCNC(=O)c1c(NC(=O)C2C(C)(C)C2(C)C)sc2c1CCCC2
Reaction #176796
DOI: 10.1039/C8SC04228D
COc1ccc(CN2CCc3c(sc(N)c3C(=O)OC(C)(C)C)C2CNC(=O)c2cn(Cc3ccccc3)c3ccccc23)cc1
Reaction #178482
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(NC(C)=O)sc2c1CCCC2
Reaction #187154
DOI: 10.1039/C8SC04228D
CNC(=O)c1c(NC(=O)C2C(C)(C)C2(C)C)sc2c1CCCC2
Reaction #191721
DOI: 10.1039/C8SC04228D
CCOC(=O)c1csc(CC)c1
Reaction #194956
DOI: 10.1039/C8SC04228D
CC(=O)N(Cc1ccccc1)CC1c2sc(N)c(C(=O)OC(C)(C)C)c2CCN1C(C)c1ccccc1
Reaction #200253
DOI: 10.1039/C8SC04228D
CCCOC(=O)c1c(NC(=O)c2c(F)cccc2C(F)(F)F)sc2c1C(C)(C)OC2(C)C
Reaction #208890
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)c1c(N)sc2c1CCOC2CN
Reaction #213452
DOI: 10.1039/C8SC04228D
O=C(Cn1nc(C(F)(F)F)c2c1CCCC2)Nc1sc2c(c1C(=O)O)CCCC2
Reaction #239419
DOI: 10.1039/C8SC04228D
CC1(C)C(C(=O)Nc2sc3c(c2C(=O)NCCCCCO)CCCC3)C1(C)C
Reaction #241474
DOI: 10.1039/C8SC04228D
CC(C)C(C)NC(=O)c1c(NC(=O)C2C(C)(C)C2(C)C)sc2c1CCCC2
Reaction #241542
DOI: 10.1039/C8SC04228D
COc1ccc(CN2CCc3c(sc(N)c3C(=O)OC(C)(C)C)C2CN)cc1
Reaction #243543
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(CC)sc1Nc1ccccc1[N+](=O)[O-]
Reaction #244909
DOI: 10.1039/C8SC04228D
CCC(CC)C(=O)Nc1sc2c(c1C(=O)NCc1ccccc1)CCCC2
Reaction #252010
DOI: 10.1039/C8SC04228D
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