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c1ccc([Se][Se]c2ccccc2)cc1

NC(C[Se]CC(N)c1ccccc1)c1ccccc1
Reaction #3997
Phenyl-2-aminoethyl selenide
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(=O)c2ccccc2)cc1[Se][Se]c1cc(C(=O)c2ccccc2)ccc1N
Reaction #6016
BIS(2-AMINO-5-BENZOYLPHENYL) DISELENIDE
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C[C@@H](O)[C@H]2CO[C@@H]1O2
Reaction #64318
1,6-anhydro-3-deoxy-β-D-threo-hexopyranos-2-ulose
Ausbeute 80.6%DOI: 10.6084/m9.figshare.5104873.v1
[Se]=[SeH-]
Reaction #274121
DOI: 10.1039/C8SC04228D
CC(=CN1C(=O)c2ccccc2C1=O)c1ccco1
Reaction #343563
colorless crystals
Ausbeute 299.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCNC(=O)OCC(CNS(=O)(=O)CCC([SeH])c1ccccc1)OC
Reaction #815608
2-methoxy-1-octadecylcarbamoyloxy-3-(3-phenylselenylpropylsulfonylamino)propane
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[N-]C1CCCCC1.[Li+]
Reaction #933867
Lithium cyclohexylisopropylamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCNC(=O)OCC(CNS(=O)(=O)CCC([SeH])c1ccccc1)OC
Reaction #934150
2-methoxy-1-octadecylcarbamoyloxy-3-(3-phenylselenylpropylsulfonylamino)propane
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(NC(=O)c1sc(Cl)cc1Cc1cccc(Cl)c1)c1ccc(C#N)cc1
Reaction #957219
desired product
DOI: 10.6084/m9.figshare.5104873.v1
NC(C[Se]CC(N)c1ccccc1)c1ccccc1
Reaction #1252186
Phenyl-2-aminoethyl selenide
DOI: 10.6084/m9.figshare.5104873.v1
NC(C[Se]CC(N)c1ccccc1)c1ccccc1
Reaction #1467279
Phenyl-2-aminoethyl selenide
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1548196
selenide
DOI: 10.6084/m9.figshare.5104873.v1
NC(C[Se]CC(N)c1ccccc1)c1ccccc1
Reaction #1654330
DOI: 10.1039/C8SC04228D
—
Reaction #1821889
selenide
DOI: 10.6084/m9.figshare.5104873.v1
OCc1cc(F)ccc1[Se][Se]c1ccc(F)cc1CO
Reaction #2162964
2,2′-diselenobis(5-fluorobenzyl alcohol)
DOI: 10.6084/m9.figshare.5104873.v1