33163-29-0Relevant academic research and scientific papers
Concise synthesis of cyclic carbonyl compounds from haloarenes using phenyl formate as the carbonyl source
Konishi, Hideyuki,Nagase, Hiroki,Manabe, Kei
, p. 1854 - 1857 (2015)
Various cyclic carbonyl compounds were concisely synthesized by carbonylative cyclization of haloarenes bearing nucleophilic moieties under Pd catalysis. A broad substrate scope and a feasible large-scale synthesis clearly demonstrate the high applicability of the reaction as a general, user-friendly method for access to cyclic carbonyl compounds.
Acylanthranils. 11. Reaction of Acylanthranils with Alcohols To Give the Corresponding Esters
Errede, L.A.,Ashley, P.E.,McBrady, J.J.,Yarian, D.R.
, p. 3825 - 3828 (2007/10/02)
Although the reactions of acetylanthranil (1, R = CH3) with nucleophilic molecules of the type HNu usually occur "abnormally" via nucleophilic attack at the less electropositive center, C-2 (pathway A, Scheme II), it was shown that reactions of 1 with the anion form, Nu(1-), always occur "normally" via nucleophilic attack at the more electropositive center, C-4 (pathway B, Scheme II).Thus, reaction of 1 with ROH in the presence of a small amount of RO(1-) gives the corresponding o-acetamidobenzoate ester 4 in very good yields, rather than the corresponding acetimidate 3.These results are consistent with the hypothesis that the "abnormal" selectivity is attributable to formation of a molecular complex, 1*(HNu)n, via hydrogen bonding with the heterocyclic nitrogen atom of 1, which favors subsequent nucleophilic attack at the adjacent electropositive center at C-2.Since Nu(1-) cannot be restrained by the tether of hydrogen bonding to the electron donating atoms of 1, reaction occurs "normally" via direct nucleophilic attack at C-4.
