部分構造検索

O=C(O)CCCCCBr

CCOC(=O)CCCCCOc1ccc(N(C(=O)OC(C)(C)C)c2ccncc2)cc1
Reaction #2334
ethyl 6-[4-[N-(4-pyridyl)-N-tertiary-butyloxycarbonylamino]phenoxy]hexanoate
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(C(=O)O)C1C(C(Cl)(Br)C(F)(F)F)S(C)(=O)=O
Reaction #5737
2,2-dimethyl-3-[2-trifluoromethyl-2-bromo-2-chloro-1-methylsulfonylethyl]-cyclopropane carboxylic acid
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
COC(=O)[C@@H]1C[C@@H](Br)C(=O)[C@@H]2[C@@]3(C)C[C@@H](c4ccoc4)OC(=O)[C@H]3CC[C@]21C
Reaction #40600
36
収率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](N=[N+]=[N-])C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40601
38
収率 87.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCBr
Reaction #47709
product
収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCBr
Reaction #47712
product ( 1 )
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCCCOc1c(OC)ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)oc12
Reaction #48940
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)CCCCCOc1ccc2nc(-c3ccccc3)n(Cc3ccccc3)c2c1
Reaction #52168
1-Benzyl-2-phenyl-6-[(5-(iso-propyl-oxycarbonyl)pentyl]oxy]-benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1c(OCCCCCC(=O)O)ccc(Cl)c1Cl
Reaction #63245
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCc1c(OCCCCCC(=O)O)ccc(Cl)c1Cl
Reaction #63252
desired title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCCCOc1ccc(Cl)c(Cl)c1CCO
Reaction #63253
6-[2-(2-hydroxyethyl)-3,4dichlorophenoxy]hexanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1ccccc1)OC(=O)C[C@H](O)C[C@H](O)CBr
Reaction #67677
crude title compound
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
O=C(O)C12CC[C@H](CC1Br)C2
Reaction #74389
(4S)-2-bromobicyclo[2.2.1]heptane-1-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C12CCC(CC1)C2
Reaction #74390
bicyclo[2.2.1]heptane-1-carboxylic acid
収率 81.3%DOI: 10.6084/m9.figshare.5104873.v1
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