Поиск подструктуры

241740

CCC1(CO)OCCO1
Reaction #59935
title compound
Выход 71.5%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(COc2ccnc(CS(=O)c3nc4ccccc4[nH]3)c2C)OCCO1.[Na]
Reaction #59936
title compound
Выход 9.6%DOI: 10.6084/m9.figshare.5104873.v1
COCC1(CCO)OCCO1
Reaction #59940
title compound
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC1(CCOc2ccnc(CS(=O)c3nc4ccccc4[nH]3)c2C)OCCO1.[Na]
Reaction #59941
title compound
Выход 3.9%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(COCC2(CCC3SCCCS3)OCCO2)cc1
Reaction #204271
DOI: 10.1039/C8SC04228D
c1ccc(COCC2(CCC3SCCCS3)OCCO2)cc1
Reaction #214739
1-benzyloxy-2,2-ethylenedioxy-4-(1,3-dithian-2-yl)-butane
DOI: 10.6084/m9.figshare.5104873.v1
CSCOC(C)(CCCC(C)CO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)C(=O)CCC1(COS(=O)(=O)c2ccc(C)cc2)OCCO1
Reaction #214740
11-t-butyldiphenylsiloxy-6,10-dimethyl-2,2-ethylenedioxy-6-methylthiomethoxy-5-oxo-1-tosyloxyundecane
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CSCOC(C)(CCCC(C)CO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)C(O)CCC1(COS(=O)(=O)c2ccc(C)cc2)OCCO1
Reaction #214741
11-t-butyldiphenylsiloxy-6,10-dimethyl-2,2-ethylenedioxy-5-hydroxy-6-methylthiomethoxy-1-tosyloxyundecane
Выход 97.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C=O)CCCC1(C)OCC2(CCC1OCc1ccccc1)OCCO2
Reaction #214747
3-benzyloxy-6,6-ethylenedioxy-2-methyl-2-(4'-methyl-5'-oxopentyl)-oxepane
Выход 83.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(CCCCOCc2ccccc2)CCCC2(CO1)OCCO2
Reaction #292274
DOI: 10.1039/C8SC04228D
O=C1CC2C(CC(O)C2CCC2(COc3cccc(Cl)c3)OCCO2)O1
Reaction #293282
DOI: 10.1039/C8SC04228D
OC1CC2(CO1)OCCO2
Reaction #345340
Compound 7
Выход 85.7%DOI: 10.6084/m9.figshare.5104873.v1
C=C[C@@H](OCOCCOC)[C@H](O)CC1(CO[Si](C)(C)C(C)(C)C)OCCO1
Reaction #345341
Compound 10-1
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C[C@@H]2[C@@H](CCC3(COc4cccc(Cl)c4)OCCO3)[C@H](O)C[C@@H]2O1
Reaction #363006
10
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](O[C@@H]1C[C@@H]2OC(=O)C[C@@H]2[C@H]1CCC1(COc2cccc(Cl)c2)OCCO1)(c1ccccc1)c1ccccc1
Reaction #363007
11
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](O[C@@H]1C[C@@H]2OC(O)C[C@@H]2[C@H]1CCC1(COc2cccc(Cl)c2)OCCO1)(c1ccccc1)c1ccccc1
Reaction #363008
12
Выход 100.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C=O)CCCC1(C)CCCC2(CO1)OCCO2
Reaction #372229
DOI: 10.1039/C8SC04228D
CC(C)OC(=O)CCCCCC[C@@H]1[C@@H](C=O)OCC12OCCO2
Reaction #448816
aldehyde
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1
OC1C[C@@H]2[C@@H](CCC3(COc4ccccc4)OCCO3)[C@H](O)C[C@@H]2O1
Reaction #459298
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(COC2CCC3(CC2)OCCO3)cc1
Reaction #486289
benzyl ether
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
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