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88573

O=[N+]([O-])c1c(CBr)cc(CBr)cc1CBr
Reaction #5648
nitro
Выход 86.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc(C(=O)O)nc(C(=O)O)c2)c(OC)c1
Reaction #5649
SiO2
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C=Cc2cc(C=Cc3cc(C(C)(C)C)cc(C(C)(C)C)c3)cc(CBr)c2)cc(C(C)(C)C)c1
Reaction #6676
3,5-bis(3′,5′-di-tert-butylstyryl)benzyl bromide
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(CBr)cc(C(=O)OCC)c1
Reaction #42300
ethyl 3-(bromomethyl)-5-[(dipropylamino)carbonyl]benzoate
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(CC#N)cc(C(=O)OCC)c1
Reaction #42301
ethyl 3-(cyanomethyl)-5-[(dipropylamino)carbonyl]benzoate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(F)(F)F)cc1CNCc1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #45310
[2-amino-5-(trifluoromethyl)benzyl][3,5-bis(trifluoromethyl)benzyl]amine
Выход 24.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #45329
EtOAc hexanes
Выход 25.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #65517
2.129
Выход 68.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #65518
2.27
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #65519
1.063
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Oc1c(C)cc(CBr)cc1C)c1cccc(Cl)c1
Reaction #65521
title compound
Выход 82.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1c(C)cc(CBr)cc1C
Reaction #71568
title compound
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1c2ccc(C(F)(F)F)cc2[C@@H](N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)C(=O)OC)C[C@H]1CC
Reaction #77864
title compound
Выход 55.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc2c1c1c(n2Cc2cc(C)cc(C)c2)CCCC1=O
Reaction #79685
9-[(3,5-dimethylphenyl)methyl]-5-carbomethoxy-1,2-dihydrocarbazol-4(3H)-one
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCC(CO)O1.FC(F)(F)c1cc(COCc2cc(C(F)(F)F)cc(C(F)(F)F)c2)cc(C(F)(F)F)c1
Reaction #83414
2,2-dimethyl- 1,3-dioxolane-4-methanol 3,5-bistrifluoromethylbenzyl ether
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)Cc1cc(CC(=C)C)cc(-c2nc3ncccc3o2)c1
Reaction #94665
2-[3,5-di(2-methylallyl)phenyl]oxazolo[4,5-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1cccc(OCc2cc(C)cc(C)c2)c1
Reaction #160640
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(C#Cc2cc(CBr)c3c(c2)C(C)(C)CC(C)(C)O3)cc1
Reaction #177159
DOI: 10.1039/C8SC04228D
COC(=O)Cc1ccc(C#Cc2cc(C(C)(C)C)c(OC(C)C)c(CBr)c2C)cc1
Reaction #178153
DOI: 10.1039/C8SC04228D
COC(=O)C1CCC(NCc2cc(C(F)(F)F)cc(C(F)(F)F)c2)C1c1ccc(F)cc1
Reaction #178267
DOI: 10.1039/C8SC04228D
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