454186-07-3Relevant academic research and scientific papers
Intramolecular biaryl coupling reaction of benzyl benzoate and phenyl benzoate derivatives, and its application to the formal synthesis of (-)-steganone
Takeda, Shigemitsu,Abe, Hitoshi,Takeuchi, Yasuo,Harayama, Takashi
, p. 396 - 408 (2007/10/03)
Construction of the biaryl moiety of stegane and related compounds through an intramolecular biaryl coupling reaction is described. Undesired products were obtained by the intramolecular coupling reaction of benzyl benzoates (8, 13, and 14) because of the
First enantioselective total synthesis of (-)-tejedine
Wang, You-Chu,Georghiou, Paris E.
, p. 2675 - 2678 (2007/10/03)
(Matrix presented) The first enantioselective total synthesis of (-)-tejedine (1) is reported. Tejedine is a seco-bisbenzyltetrahydroisoquinoline isolated in 1998 as a minor component from Berberis vulgaris. The synthesis was achieved using a strategy employing four key steps, including a chiral auxiliary-assisted diastereoselective Bischler-Napieralski cyclization.
