子结构搜索

7114

CCOC(=O)c1cc(CC)cnc1C(=O)OCC
Reaction #4014
title product
收率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(CC)cnc1C
Reaction #4015
title product
收率 43.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2ncnn2c(O)c1Cl
Reaction #11292
5-Chloro-4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cl)=NNc1ccc(Cl)cc1
Reaction #48033
ethyl 2-chloro[(4-chlorophenyl)hydrazono]acetate
收率 73.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cl)C(=O)CC
Reaction #55098
ethyl 2-chloro-3-oxopentanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cl)C(=O)CC
Reaction #55767
ethyl 2-chloro-3-oxopentanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1oc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)nc1C
Reaction #71897
title compound
收率 31.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cl)C(=O)c1ccccc1
Reaction #75953
product
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N)nc1-c1ccccc1
Reaction #75954
ethyl 2-amino-4-phenyl-1,3-thiazole-5-carboxylate
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(-c2ccc(C)cc2)nc1C
Reaction #86826
ethyl 4-methyl-2-p-tolylthiazole-5-carboxylate
收率 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)nc2c(OCC3CCCCC3)cc(C)cn12
Reaction #92678
ethyl 8-(cyclohexylmethoxy)-2,6-dimethylimidazo[1,2-a]pyridine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C(Cl)(Cl)Cl)nc(O)c1Cl
Reaction #94998
5-Chloro-4-Hydroxy-6-Methyl-2-Trichloromethylpyrimidine
收率 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1oc(N)nc1C
Reaction #157410
ethyl 2-amino-4-methyloxazole-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CCC2(C3CCCC3)CC(O)=C(Sc3nnc(CN(C)C)n3C)C(=O)O2)cc1Cl
Reaction #180732
DOI: 10.1039/C8SC04228D
CCOC(=O)C(Cl)=NNc1ccc(Cl)cc1
Reaction #183644
DOI: 10.1039/C8SC04228D
O=C(CCc1ccco1)NCCC1(C2CCCC2)CC(=O)C(Cl)C(=O)O1
Reaction #184110
DOI: 10.1039/C8SC04228D
Cc1cc(C)n2nc(SC3=C(O)CC(CCNC(=O)CCc4ccco4)(C4CCCC4)OC3=O)nc2n1
Reaction #185359
DOI: 10.1039/C8SC04228D
CCOC(=O)C(OC(=O)c1ccc(C(F)(F)F)cc1)C(=O)C(C)C
Reaction #185993
DOI: 10.1039/C8SC04228D
COc1ccc(CCC2(C3CCCC3)CC(O)=C(Sc3nc(C)cc(C)c3C#N)C(=O)O2)cc1Cl
Reaction #191196
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C(C)=O)n1nc(C(F)(F)F)nc1C
Reaction #191483
DOI: 10.1039/C8SC04228D
第 1 页下一页