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The 1,3-dipolar cycloaddition of 1-methylphthalazinium ylides to non-symmetrically activated alkynes on a solid support under microwave irradiation
Author(s) -
Ştefan Dima,
Gheorghita Zbangioc,
Ionel I. Mangalagiu
Publication year - 2006
Publication title -
journal of the serbian chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.227
H-Index - 45
eISSN - 1820-7421
pISSN - 0352-5139
DOI - 10.2298/jsc0602103d
Subject(s) - regioselectivity , catalysis , microwave irradiation , cycloaddition , interphase , microwave , chemistry , irradiation , solvent , photochemistry , organic chemistry , physics , genetics , quantum mechanics , nuclear physics , biology
In this paper, a comparative study of the reaction of 1-methylphthalazini- um ylides with non-symmetrically activated alkynes in a solid medium by classical heating and under microwaves is presented. The reactants were impregnated on a mineral support (Al2O3 - KF) or were brought into catalytic conditions through interphase solid - liquid transfer in the absence of a solvent and were then subjected to microwave irradiation. The reaction of 1-methylphthalazinium ylides with non- symmetrically activated alkynes on a mineral support and in phase transfer catalysis under microwave irradiation is a regioselective reaction and results in larger yields in a shorter time than under classical conditions.

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