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Synthessi of 3-Benzyl-1,3-thiazolidines by {2+3}-Cycloaddition of Sonochemically Generated Azomethine Ylides with Thiocarbonyl Compounds

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Sonification of N-benzyl-N-(methoxymethyl)-N-[(trimethylsilyl)methyl]amine (5a) in the presence of LiF led to the formation of the reactive azomethine ylide 1d, which was intercepted by cyclic thioketones to give spirocyclic 1,3-thiazolidines. In the case of 2,2,4,4-tetramethylcyclobutane-1,3-dithione (13), the 1:1- and 1:2-cycloadduct, respectively, was formed as the major product depending on the ratio of the starting materials. With 1,3-thiazole-5(4H)-thiones, 1d undergoes stereoselective [2+3]-cycloadditions with the C=S group to yield spirocyclic 1:1-adducts. In the case of the 1,3-dipole generated from N-benzyl-N-(methoxymethyl)-N-[1-(trimethylsilyl)ethyl]amine (5b), the [2+3]-cycloaddition proceeded in a non-regioselective manner leading to a mixture of regio- and diastereoisomers.
Rocznik
Strony
867--879
Opis fizyczny
Bibliogr. 52 poz., rys.
Twórcy
autor
  • Organisch-chemisches Institut der Universität Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland
autor
  • Organisch-chemisches Institut der Universität Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland
autor
  • Section of Heteroorganic Compounds, University of Łódź, Narutowicza 68, PL-90-136 Łódź, Poland
  • Organisch-chemisches Institut der Universität Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland
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Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ1-0021-0047
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