部分構造検索

CCOC(=O)CCCBr

CCOC(=O)CCCOc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #2302
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(C)COc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #2339
ethyl 3-methyl-4-[4-[4-(4-pyridyl)piperazin-1-yl]phenoxy]butyrate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1csc(N)n1
Reaction #2724
Ethyl 2-amino-thiazol-4-yl-glyoxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(SCCCC(=O)O)cc(C(C)(C)C)c1O
Reaction #5596
4-[[3,5-bis(1,1-dimethylethyl)-4-hydroxy phenyl]thio]butanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](C(=O)OC(C)(C)C)N1CCC(N=[N+]=[N-])C1=O
Reaction #7372
title compound
収率 18.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCNC(CC)C(=O)OC(C)(C)C)N=[N+]=[N-]
Reaction #7392
title compound
収率 52.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCNc1cc(Cl)cnc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11814
title compound
収率 36.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCc2sc(NC(=N)N)nc21
Reaction #40318
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCC(Br)C1=O
Reaction #40319
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCc2nc(NC(=N)N)sc2C1
Reaction #40321
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCC(=O)C(Br)C1
Reaction #40322
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(c2ccccc2)CCC(=O)C(Br)C1
Reaction #40326
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCOc1c(OC)ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)oc12
Reaction #48938
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCON1C(=O)c2ccccc2C1=O
Reaction #49025
4-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-butyric acid ethyl ester
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC=Cc1cccc(OCc2c(C)cccc2C)c1
Reaction #53313
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Br.CCOC(=O)C(=NOC)c1csc(N)n1
Reaction #56563
ethyl 2-methoxyimino-2-(2-aminothiazol-4-yl)acetate hydrobromide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCN[C@@H](Cn1c(=O)c(-c2cccc(OC)c2F)c(C)n(Cc2c(F)cccc2C(F)(F)F)c1=O)c1ccccc1
Reaction #56773
1g
収率 49.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCN[C@@H](Cn1c(=O)c(-c2cccc(OC)c2Cl)cn(Cc2c(F)cccc2C(F)(F)F)c1=O)c1ccccc1
Reaction #56791
compound 7i
収率 53.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCN[C@H](CC(C)C)Cn1c(=O)c(-c2cccc(OC)c2Cl)cn(Cc2c(F)cccc2C(F)(F)F)c1=O
Reaction #56793
compound 8c
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCOc1ccc2c(c1)C(C#CC1CC1)(C(F)(F)F)OC(=O)N2
Reaction #57293
10
収率 39.3%DOI: 10.6084/m9.figshare.5104873.v1
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