377198

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Synlett, 143-143 (1993)

Journal of the American Chemical Society, 115, 1187-1187 (1993)

Regiochemistry of the photostimulated reaction of the phthalimide anion with 1-iodoadamantane and tert-butylmercury chloride by the S(RN)1 mechanism.

Manuel Bajo Maquieira et al.

The Journal of organic chemistry, 67(3), 1012-1015 (2002-02-22)

The photostimulated reaction of the phthalimide anion (1) with 1-iodoadamantane (2) gave 3-(1-adamantyl) phthalimide (3) (12%) and 4-(1-adamantyl) phthalimide (4) (45%), together with the reduction product adamantane (AdH) (21%). The lack of reaction in the dark and inhibition of the

Photostimulated reaction of 1-iodoadamantane with carbanionic nucleophiles in DMSO by the SRN1 mechanism.

Borosky GL, et al.

The Journal of Organic Chemistry, 55(12), 3705-3707 (1990)

[1-(1-Adamantylamino)ethyl-idene]oxonium methane-sulfonate.

Robert Vícha et al.

Acta crystallographica. Section E, Structure reports online, 65(Pt 6), o1307-o1307 (2009-01-01)

In the title salt, C(12)H(20)NO(+)·CH(3)SO(3) (-), the [1-(1-adamantyl-amino)ethyl-idene]oxonium cations and methane-sulfonate anions are linked into chains along the a axis via O-H⋯O and N-H⋯O hydrogen bonds. All non-H atoms of the acetamido group are essentially planar, with a maximum deviation

Rate study of haloadamantane reduction by samarium diiodide.

Lin T-Y, et al.

J. Chin. Chem. Soc., 49(6), 969-973 (2002)

Electrosynthetic reduction of 1-iodoadamantane forming 1,1'-biadamantane and adamantane in aprotic solvents: insonation switches the mechanism from dimerisation to exclusive monomer formation.

Christopher A Paddon et al.

Ultrasonics sonochemistry, 14(5), 502-508 (2007-01-17)

The combination of ultrasound and electrochemistry -sonoelectrochemistry can produce a variety of effects within an electrochemical system including enhanced mass transport, in situ cleaning of an electrode surface, diminution of the diffusion layer, and possible induction of new reactions by

Dimerization of Cubene. 1-Iodoadamantane as a Probe for Radical Intermediates.

Lukin K and Eaton PE.

Journal of the American Chemical Society, 117(29), 7652-7656 (1995)

Fluorescent quenching of the 2-naphthoxide anion by aliphatic and aromatic halides. Mechanism and consequences of electron transfer reactions.

Juan E Argüello et al.

The Journal of organic chemistry, 68(6), 2362-2368 (2003-03-15)

The fluorescent excited state of the 2-naphthoxide ion (1) is quenched by aliphatic and aromatic halides according to an electron-transfer mechanism, with generation of the corresponding alkyl and aryl radicals by a concerted or consecutive C-X bond fragmentation reaction. Whereas

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