550348-84-0Relevant articles and documents
Catalytic crossed Michael cycloisomerization of thioenoates: total synthesis of (+/-)-ricciocarpin A.
Agapiou, Kyriacos,Krische, Michael J
, p. 1737 - 1740 (2003)
[reaction: see text] Thioenoates are found to participate in highly chemoselective catalytic crossed Michael cycloisomerization with appendant aryl ketone and enoate partners to afford cyclopentene and cyclohexene products. This methodology has enabled a