909914-55-2Relevant academic research and scientific papers
Short synthesis of (+)-cylindricine C by using a catalytic asymmetric Michael reaction with a two-center organocatalyst
Shibuguchi, Tomoyuki,Mihara, Hisashi,Kuramochi, Akiyoshi,Sakuraba, Shun,Ohshima, Takashi,Shibasaki, Masakatsu
, p. 4635 - 4637 (2007/10/03)
(Chemical Equation Presented) Two for the price of one: The total synthesis of (+)-cylindricine C has been achieved in six steps using a catalytic asymmetric Michael reaction and tandem cyclization. A newly designed two-center organocatalyst gives good selectivity in this Michael reaction. TaDiAS = tartrate-derived diammonium salt.
