部分構造検索

COCCBr

CCOC(=O)C(CC)N1CC(c2ccccc2)CCC1=O
Reaction #7495
ester
収率 70.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)/C(Br)=N/Nc1ccccc1Cl
Reaction #7501
title compound
収率 71.3%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)C(CC)Nc1ccc2ccccc2c1
Reaction #51328
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1OC(CNc2ccccc2OC)OC1C
Reaction #56319
N-(4-methyl-5-ethyl-1,3-dioxolan-2-ylmethyl)-2-methoxyaniline
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1ccccc1)OC(=O)C[C@H]1C[C@@H](CBr)OC(C)(C)O1
Reaction #67679
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1SC(NC2CC3CCC2C3)=NC1=O
Reaction #74315
2-(bicyclo[2.2.1]hept-2-ylamino)-5-ethyl-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CCC1SC(NC2CCCCC2)=NC1=O
Reaction #74317
2-(cyclohexylamino)-5-ethyl-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #86630
compound 5
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2ccc(C#N)cc2[C@@H](N2CCCC2=O)[C@@H]1O
Reaction #93186
title compound
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Br)Cc1cccc(Cl)c1Cl
Reaction #94009
methyl 2-bromo-3-(2,3-dichlorophenyl)propionate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(Oc1cccc([N+](=O)[O-])c1)C(=O)OCC
Reaction #158528
diethyl 2-methyl-2-(3-nitrophenoxy)malonate
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1Oc2c(Br)cccc2NC1=O
Reaction #163523
8-bromo-2-ethyl-2H-benzo[b][1,4]oxazin-3(4H)-one
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(Oc1cccc([N+](=O)[O-])c1)C(=O)OCC
Reaction #163637
diethyl 2-methyl-2-(3-nitrophenoxy)malonate
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC)Oc1ccc2c(-c3ccc(Cl)cc3)noc2c1
Reaction #187630
DOI: 10.1039/C8SC04228D
COC(=O)C(Br)c1cccc(C(F)(F)F)c1
Reaction #191975
DOI: 10.1039/C8SC04228D
CC1(C)Oc2ccc(C#N)cc2C(OC(=O)C2CCCN2S(=O)(=O)c2ccc([N+](=O)[O-])cc2)C1Br
Reaction #194838
DOI: 10.1039/C8SC04228D
Clc1ccc2c(c1)C(OCCBr)c1cc(Cl)ccc1OCO2
Reaction #197985
DOI: 10.1039/C8SC04228D
c1ccc(CNCC2Cc3ccccc3O2)cc1
Reaction #198627
DOI: 10.1039/C8SC04228D
CS(=O)(=S)OCCOCCOCCOC(=O)c1ccc(N)cc1
Reaction #199278
DOI: 10.1039/C8SC04228D
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