63075-56-9Relevant academic research and scientific papers
A Novel Method of Annulation through α,β-Epoxy Sulfoxides with the Aid of Intramolecular Radical Cyclization
Satoh, Tsuyoshi,Itoh, Masayuki,Yamakawa, Koji
, p. 1949 - 1950 (2007/10/02)
A novel method of annulation was realized from ketones through α,β-epoxy sulfoxides with the aid of endo-type intramolecular radical cyclization.In these reactions 1-chloroalkyl phenyl sulfoxides having phenylseleno group on an end of the alkyl group acted as synthons of the annulation.
"1,4" Alkyl Migrations in Fischer Indole Cyclizations
Miller, Bernard,Matjeka, Edward R.
, p. 4772 - 4780 (2007/10/02)
The product from Fisher indole cyclization and dehydrogenation of cyclohexanone 2,4,6-trimethylphenylhydrazone (1) was determined to be 2,3,4-trimethylcarbazole (3) resulting from a formal 1,4-methyl migration, as previously proposed.To determine the destinations of migrating groups in these rearrangements, the Fischer indole cyclization and dehydrogenation of cyclohexanone 2-ethyl-6-methylphenylhydrazone (17) were studied.The products obtained were 1-ethylcarbazole, 1-methylcarbazole, 2-ethyl-1-methylcarbazole (18), and an apparent mixture of 1-ethyl-4-methylcarbazole (21) and 4-ethyl-1-methylcarbazole (22).However, no 1-ethyl-2-methylcarbazole (19), which would have been obtained by a "1,4"-methyl migration, was obtained.Analysis of the product ratios suggested that the apparent ethyl shift in formation of 18 actually proceeded by a formal shift of either an ethyl or a methyl group, followed by a ethyl shift.Cyclization of 3-pentanone 2,4,6-trimethylphenylhydrazone (26) proceeded to give the product of "1,4" methyl migration, demonstrating that such reactions can occur with phenylhydrazones of ketones other than cyclohexanone.It is proposed that steric factors play a major role in determining whether migrating groups undergo or "1,4" shifts during Fischer indole cyclizations.
