150674-67-2Relevant academic research and scientific papers
An Enantioselective Synthesis of (-)-α-Kainic Acid via Thiyl Radical Addition-Cyclization-Elimination Reaction
Miyata, Okiko,Ozawa, Yoshiki,Ninomiya, Ichiya,Naito, Takeaki
, p. 275 - 276 (1997)
An enantioselective synthesis of (-)-α-kainic acid has been achieved via the route involving thiyl radical addition-cyclization-elimination reaction.
Radical cyclization in heterocycle synthesis. Part 10: A concise synthesis of (-)-kainic acid via sulfanyl radical addition-cyclization-elimination reaction
Miyata, Okiko,Ozawa, Yoshiki,Ninomiya, Ichiya,Naito, Takeaki
, p. 6199 - 6207 (2007/10/03)
Sulfanyl radical addition-cyclization-elimination of diallylamines in the presence of thiophenol and AIBN gave the 2,3,4-trisubstituted pyrrolidine in high yield. This reaction was extended to a radical cyclization using a catalytic amount of thiophenol. A successful application was demonstrated by the asymmetric synthesis of (-)-kainic acid. (C) 2000 Elsevier Science Ltd.
A Total Synthesis of (-)-α-Kainic Acid Involving a Pauson-Khand Reaction as the Key Step
Yoo, Sung-eun,Lee, Sang Hee
, p. 6968 - 6972 (2007/10/02)
A synthetic route to (-)-α-kainic acid has been developed based on the Pauson-Khand reaction as a key step for the construction of the bicyclic ring system.In this reaction a built-in oxazolidinone ring serves as a rigid template for good diastereofacial selectivity.
A Total Synthesis of (-)-α-Kainic Acid By the Pauson-Khand Reaction
Yoo, Sung-eun,Lee, Sang-Hee,Jeong, Nakcheol,Cho, Inho
, p. 3435 - 3438 (2007/10/02)
A total synthetic route to (-)-α-kainic acid has been developed based on the Pauson-Khand reaction as a key reaction for the construction of the bicyclo ring system.
