Rearrangement of carbocations derived from 1,8-bis(dimethylamino)naphthyl-2-methanols into 4-R-1,1,3-trimethyl-2,3-dihydroperimidinium salts
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference20 articles.
1. Tris(1-naphthyl)- and tris(2-naphthyl)methyl cations: highly crowded triarylmethyl cations 1
2. Preparation of Condensed Aromatics by Superacidic Dehydrative Cyclization of Aryl Pinacols and Epoxides1a
3. The effects of cyclic terminal groups in di- and tri-arylmethane dyes. Part 2.1 Steric and electronic effects in derivatives of Victoria Blue
4. Synthesis and Reactivity of a 1,8-Bis(methylium)naphthalenediyl Dication
5. peri-Interaction between diarylmethyl and diarylmethylium units in 1,8-disubstituted naphthalenes: preference of localized structure for the C–H bridged carbocation
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1. Perimidines: a unique π-amphoteric heteroaromatic system;Russian Chemical Reviews;2020-11-01
2. The first proton sponge-based amino acids: synthesis, acid–base properties and some reactivity;Organic & Biomolecular Chemistry;2015
3. Proton Sponges and Hydrogen Transfer Phenomena;Mendeleev Communications;2012-05
4. Naphthalene proton sponges as hydride donors: diverse appearances of the tert-amino-effect;Organic & Biomolecular Chemistry;2011
5. tert-Amino Effect in peri-Substituted Naphthalenes: Syntheses of Naphthazepine and Naphthazonine Ring Systems;Synlett;2010-07-30
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