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675634

COc1ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)oc2c1OCCCCCCC(=O)O
Reaction #48963
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CCCCCCBr
Reaction #95932
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=CCCCCCCBr
Reaction #95933
title compound
Rendimiento 85.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCCCCC(C(=O)CC)C(=O)OCC
Reaction #177256
DOI: 10.1039/C8SC04228D
CCCCOC(=O)C1(CCCCCBr)CCCC1
Reaction #182522
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCCCn1ccc(-c2ccccc2O)n1
Reaction #187675
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCCCOc1c(I)cc(I)cc1I
Reaction #201125
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCCCn1c(C)nc(-c2ccccc2)c1-c1ccccc1
Reaction #202857
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCCCOc1cccc(OC)c1C=O
Reaction #210733
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCCC(C(=S)OCC)c1ccccc1
Reaction #213925
Diethyl α-Phenylthiosuberate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCCCCN(C)Cc1ccccc1
Reaction #236232
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #253297
DOI: 10.1039/C8SC04228D
CC(CO)(CCCCCBr)c1ccccc1
Reaction #260023
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCCCN(CCOc1cc(Cl)cc(Cl)c1)S(C)(=O)=O
Reaction #262912
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCCCC(C(C)=O)C(C)=O
Reaction #265985
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C)(C)CCCCCBr
Reaction #279290
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCCCOc1ccc(-c2cnc3ccc(-c4cn(C(c5ccccc5)(c5ccccc5)c5ccccc5)nc4-c4ccc(F)cc4)cn23)cc1
Reaction #292430
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C)(C)CCCCCBr
Reaction #299318
DOI: 10.1039/C8SC04228D
CCOC(=O)CC12CCC1CC=C(Br)C2=O
Reaction #300543
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCCCn1cc(CN(C(=O)C2CCCc3c(OCc4ccccc4)cccc32)c2ccc(C(C)C)nc2)cn1
Reaction #305970
ethyl 7-(4-{[N-(5-benzyloxy-1,2,3,4-tetrahydronaphthalen-1-ylcarbonyl)-N-(6-isopropylpyridin-3-yl)amino]methyl}pyrazol-1-yl)heptanoate
DOI: 10.6084/m9.figshare.5104873.v1
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