83504-95-4Relevant academic research and scientific papers
6-exo-trig Michael addition-lactonizations for catalytic enantioselective chromenone synthesis
Neyyappadath, Rifahath M.,Cordes, David B.,Slawin, Alexandra M. Z.,Smith, Andrew D.
supporting information, p. 2555 - 2558 (2017/03/09)
The catalytic enantioselective 6-exo-trig Michael addition-lactonization of enone-acid substrates to form cis-chromenones with high diastereo- and enantiocontrol was developed using the commercially available isothiourea tetramisole. An acidic workup prov
SYNTHESIS OF SOME THIOACETAMIDES BY THE VILGERODT - KINDLER REACTION
Kuliev, A. B.,Anave, P. A. L.,Kuliev, F. A.,Mamedova, Sh. E.
, p. 1493 - 1494 (2007/10/02)
Some 2-hydroxy-4- and 2-hydroxy-5-methylphenylthioacetamides were synthesized by the Vilgerodt-Kindler reaction of 2-hydroxy-4- and 2-hydroxy-5-methylacetophenones with sulfur and various amines.
