部分構造検索

ClCCCCOC1CCCCO1

ClCCCCOC1CCCCO1
Reaction #5310
title compound
収率 89.9%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)[nH]c2c(c1=O)CN(CCCCOC1CCCCO1)CC2
Reaction #213469
DOI: 10.1039/C8SC04228D
CCCOC(=O)CCCCCCC1C(Cl)CC(OC2CCCCO2)C1C=O
Reaction #403269
DOI: 10.1039/C8SC04228D
CC(C)=CCC(C)[C@H](O)/C=C/[C@@H]1[C@@H](C/C=C\CCCC(=O)O)[C@H](Cl)C[C@H]1O
Reaction #413363
title compound
収率 14.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC/C=C\C[C@@H]1[C@@H](/C=C/[C@@H](OC2CCCCO2)C(C)CC=C(C)C)[C@H](OC2CCCCO2)C[C@H]1Cl
Reaction #413364
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCC(C)[C@H](O)/C=C/[C@@H]1[C@@H](C/C=C\CCCC(=O)O)[C@@H](Cl)C[C@H]1O
Reaction #413365
carboxylic acid
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCC(C)[C@H](O)/C=C/[C@@H]1[C@@H](CCCCCCC(=O)O)[C@H](Cl)C[C@H]1O
Reaction #413366
carboxylic acid
収率 43.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCC(C)[C@H](O)/C=C/[C@@H]1[C@@H](CCCCCCC(=O)NS(C)(=O)=O)[C@H](Cl)C[C@H]1O
Reaction #413368
title compound
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCC(C)[C@H](O)/C=C/[C@@H]1[C@@H](C/C=C\CCCC(=O)NS(C)(=O)=O)[C@H](Cl)C[C@H]1O
Reaction #413369
desired compound
収率 53.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCC(C)(C)[C@H](O)/C=C/[C@@H]1[C@@H](C/C=C\CCCC(=O)O)[C@H](Cl)C[C@H]1O
Reaction #413370
title compound
収率 51.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC/C=C\C[C@@H]1[C@@H](/C=C/[C@@H](OC2CCCCO2)C(C)(C)CC=C(C)C)[C@H](OC2CCCCO2)C[C@H]1Cl
Reaction #413371
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC(=O)CCCCCC[C@@H]1[C@@H](/C=C/[C@@H](O)CCC=C(C)C)[C@H](O)C[C@H]1Cl
Reaction #413372
title compound
収率 59.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCC[C@@H]1[C@@H](/C=C/[C@H](CCC=C(C)C)OC2CCCCO2)[C@H](OC2CCCCO2)C[C@H]1Cl
Reaction #413373
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C/C(Cl)=C/CC(C)[C@H](O)/C=C/[C@@H]1[C@@H](C/C=C\CCCC(=O)O)[C@H](Cl)C[C@H]1O
Reaction #413374
title compound
収率 59.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC/C=C\C[C@@H]1[C@@H](/C=C/[C@@H](OC2CCCCO2)C(C)C/C=C(/C)Cl)[C@H](OC2CCCCO2)C[C@H]1Cl
Reaction #413375
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(CCCCl)OC1CCCCO1
Reaction #459691
1-Chloro-4-(2-tetrahydropyranyloxy)nonane
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(CCCN1C(=O)c2ccccc2C1=O)OC1CCCCO1
Reaction #459692
N-[4-(2-tetrahydropyranyloxy)nonyl]phthalimide
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCO[C@H]1[C@H](O[C@H]2[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H](Cl)O[C@@H]2COC(C)=O)O[C@H](COC(C)=O)[C@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #469431
3
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCO[C@H]1[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](OC)O[C@@H]2CO)O[C@H](CO)[C@H](O)[C@@H]1O
Reaction #469432
4
収率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C)(C)[C@H](O)/C=C/[C@@H]1[C@@H](CC/C=C\CCC(=O)OC)[C@H](Cl)C[C@H]1O
Reaction #529970
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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