Michael addition reaction of thioacetic acid (AcSH) to conjugated alkenes under solvent- and catalyst-free conditions
A new and convenient procedure has been developed for the Michael addition reaction of thioacetic acid (AcSH) to a variety of conjugated alkenes under solvent- and catalyst-free conditions. These reactions proceeded in 5-60 min and produced the desired products in good to high yields. Copyright Taylor & Francis Group, LLC.
Sobhani, Sara,Rezazadeh, Soodabeh
experimental part
p. 2076 - 2084
(2010/12/19)
Novel thiol-derivatized zinc(II) phthalocyanines
Preparation and characterization of tetrasubstituted zinc(II) phthalocyanines in which sulfur is not linked to the macrocycle are reported herein for the first time. Thioacetic acid S-[3-(3,4-dicyano-phenoxy)-propyl]ester (4) was synthesized in 55% yield
García Vior, María C.,Cobice, Diego,Dicelio, Lelia E.,Awruch, Josefina
body text
p. 2467 - 2469
(2009/08/09)
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