子结构搜索

CCOC=O

Cc1oc(-c2ccc(C(F)(F)F)cc2)cc1CSc1ccc(OCC(=O)O)c(Br)c1
Reaction #9790
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CN(C2CCCCC2)c2nc(SC)ncc2C1=O
Reaction #40627
title compound
收率 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(C2CCCCC2)c2nc(SC)ncc2c1=O
Reaction #40628
title compound
收率 102.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCO[C@H]1CC[C@H](N(C)S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53947
trans-4-{4-[Methyl-(4-trifluoromethyl-benzenesulfonyl)-amino]-cyclohexyloxy}-butyric acid ethyl ester
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(C(F)(F)F)c(Cl)cc2n1-c1ccc(CCOC(=O)NS(=O)(=O)c2ccccn2)cc1
Reaction #78723
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(C(F)(F)F)c(Cl)cc2n1-c1ccc(CCOC(=O)NS(=O)(=O)c2ccncc2)cc1
Reaction #78724
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(C(F)(F)F)c(Cl)cc2n1-c1ccc(C[C@@H](C)OC(=O)NS(=O)(=O)c2ccc(C)cc2)cc1
Reaction #78726
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(C(F)(F)F)c(Cl)cc2n1-c1ccc(CCOC(=O)NS(=O)(=O)c2cccc3cnccc23)cc1
Reaction #78729
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@@H]1CCCN1C(=O)Oc1cc(F)c(C=O)c(F)c1
Reaction #155433
(S)-3,5-difluoro-4-formylphenyl 2-(acetoxymethyl)pyrrolidine-1-carboxylate
收率 50.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(C(F)(F)F)c(Cl)cc2n1-c1ccc(CCOC(=O)NS(=O)(=O)c2ccncc2)cc1
Reaction #175159
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)C2=CCN(C(=O)O)N(S(=O)(=O)c3ccc(OC)cc3)C=C2)cc1
Reaction #184542
DOI: 10.1039/C8SC04228D
CC(C)OC(=O)N=NC(=O)OC(C)C
Reaction #185200
DOI: 10.1039/C8SC04228D
CCOC(=O)C(CCO)=C(c1ccc(S(C)(=O)=O)cc1)c1cccc(F)c1
Reaction #190254
DOI: 10.1039/C8SC04228D
CCc1nc2cc(C(F)(F)F)c(Cl)cc2n1-c1ccc(CCOC(=O)NS(=O)(=O)c2ccncc2)cc1
Reaction #191775
DOI: 10.1039/C8SC04228D
CC(=O)OC1C(c2ccc(C(C)(C)C)cc2)=C(c2ccc(S(C)(=O)=O)cc2)CC1CN(C)C
Reaction #194284
DOI: 10.1039/C8SC04228D
COc1nc(C)nc(NC(=O)NS(=O)(=O)c2ccn3c2C(=O)OCC3)n1
Reaction #196038
DOI: 10.1039/C8SC04228D
CN1CCN(S(=O)(=O)c2ccc(C(CC3CCCC3)C(=O)O)cc2)CC1
Reaction #197345
DOI: 10.1039/C8SC04228D
Nc1nc2ccc(OS(=O)(=O)c3ccc(F)cc3)cc2s1
Reaction #201365
DOI: 10.1039/C8SC04228D
CCCC(NS(=O)(=O)c1ccc(Br)cc1)C(=S)Nc1ccc(CC(=O)OCC)cc1
Reaction #203238
DOI: 10.1039/C8SC04228D
CC(C)N1CC(=O)N(C)c2cnc(Nc3cc(NC(=O)NC4CCC(NC(=O)OC(C)(C)C)CC4)cc(S(C)(=O)=O)c3)nc21
Reaction #205390
DOI: 10.1039/C8SC04228D
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