Rearrangement of carbocations derived from 1,8-bis(dimethylamino)naphthyl-2-methanols into 4-R-1,1,3-trimethyl-2,3-dihydroperimidinium salts
-
Add time:07/25/2019 Source:sciencedirect.com
α-Phenylated 1,8-bis(dimethylamino)-2-naphthylmethyl carbocations have been shown to rearrange into 4-R-1,1,3-trimethyl-2,3-dihydroperimidinium cations through an intramolecular hydride shift from the 1-NMe2 group.
We also recommend Trading Suppliers and Manufacturers of 2,3-Bis(dimethylamino)-1,4,2,3-dithiadiborinane (cas 19172-56-6). Pls Click Website Link as below: cas 19172-56-6 suppliers
Prev:Oprozomib, Pomalidomide (cas 19171-19-8), and dexamethasone in patients with relapsed and/or refractory multiple myeloma
Next:Opening cobaltadicarbaborane deltahedra by external dimethylamino substituents: Conversion of icosahedra to isonido 12-vertex polyhedra) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Ultra-sensitive determination of cyanide in surface water by gas chromatography–tandem mass spectrometry after derivatization with 2-(dimethylamino)ethanethiol07/30/2019
- Synthesis and cytotoxic properties of 4,11-bis[(aminoethyl)amino]anthra[2,3-b]thiophene-5,10-diones, novel analogues of antitumor anthracene-9,10-diones07/29/2019
- Structure, bonding, and asymmetric induction in (R,R)-2,3-dimethoxy-1,4-bis(dimethylamino)butane complexes with organolithium compounds: A semiempirical computational study07/28/2019
- Palladium-catalyzed asymmetric arylation of 2,3-dihydrofuran: 1,8-Bis(dimethylamino)naphthalene as an efficient base07/27/2019
- Opening cobaltadicarbaborane deltahedra by external dimethylamino substituents: Conversion of icosahedra to isonido 12-vertex polyhedra07/26/2019


