Mizoroki-Heck reaction of 1,2-disubstituted aryl alkenes: variables of synthesis, solvent and ligand modulation of reactivity
Title | Mizoroki-Heck reaction of 1,2-disubstituted aryl alkenes: variables of synthesis, solvent and ligand modulation of reactivity |
Publication Type | Journal Article |
Year of Publication | 2020 |
Authors | Bangar, PG, Jawalkar, PR, Dumbre, SR, Raut, PK, Patil, DJ, Tv, N, Sudhakaran, S, Iyer, S |
Journal | Synthetic Communications |
Volume | 50 |
Issue | 24 |
Pagination | 3796-3803 |
Date Published | DEC |
Type of Article | Article |
ISSN | 0039-7911 |
Keywords | 12-Disubstituted aryl alkenes, 400, ligand effect, Mizoroki-Heck reaction, PEG 200, TBABr |
Abstract | Reaction of aryl iodides with 1,2-disubstituted aryl alkenes in the presence of TBABr/TBACl gave high yields of the Mizoroki-Heck product. Phosphine ligands were used for the modulation of reactivity and stereoselectivity, for the reaction of 4-iodoanisole with cinnamaldehyde. tert-Bu3P.HBF(4)gave the highest E:Z ratio of 1:0.08. The use of PEG-200 and PEG-400 as solvent could activate the reaction of aryl iodides with various 1,2-disubstituetd aryl alkenes. |
DOI | 10.1080/00397911.2020.1811986, Early Access Date = AUG 2020 |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 1.796 |
Divison category:
Organic Chemistry
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