Ortho-para selectivity in coordinated reactions of aldimines with magnesium phenoxides
โ Scribed by Giuseppe Casnati; Andrea Pochini; Giuseppe Puglia; Rocco Ungaro
- Book ID
- 104221154
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- French
- Weight
- 225 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
N-~ryl imines from aromatic aldehydes react in benzene with ortho-tertbutylphenoxymaonesium bromide to give 4,4'-arylidenebisphenols 2 through two consecutive para-regiospecific processes whereas N-alkyl imines give mainly oPthOregioselective reactions in the same conditions, producing 2,2'-arylidenebisphenols 1.
๐ SIMILAR VOLUMES
The nucleophilic addition of organic anions to aromatic compounds with halogens positioned both ortho and para to activating groups was studied in a variety of solvents. Substrates showed strong preferences for ortho substitution in most cases. Evidence is presented for activating group-dependent co