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Ortho-para selectivity in coordinated reactions of aldimines with magnesium phenoxides

โœ 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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โœฆ 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.


๐Ÿ“œ SIMILAR VOLUMES


Ortho-selectivity in SNAr substitutions
โœ Michael D. Wendt; Aaron R. Kunzer ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 431 KB

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