Determination of the absolute configurations and total synthesis of new immunosuppressants, mycestericins E and G
T Fuiita, N Hamamichi, T Matsuzaki, Y Kitao, M Kiuchi…
Index: Fujita, Tetsuro; Hamamichi, Norimitsu; Matsuzaki, Tohru; Kitao, Yuki; Kiuchi, Masatoshi; Node, Manabu; Hirose, Ryoji Tetrahedron Letters, 1995 , vol. 36, # 47 p. 8599 - 8602
Full Text: HTML
Citation Number: 30
Abstract
The absolute configurations of two new immunosuppressants, mycestericins E (1) and G (2), were establishied and both compounds were synthesized starting from 1, 8-octanediol and a fully protected methyl (2S, 4R)-oxazolidine-4-carboxylate 3. Compounds 5 and 22, with a (l'R)-hydroxyl group, were prepared from the β-keto esters 4 and 21, respectively, by stereoselective reduction with metal borohydrides.
Related Articles:
[Fairhurst, Nathan W. G.; Mahon, Mary F.; Munday, Rachel H.; Carbery, David R. Organic Letters, 2012 , vol. 14, # 3 p. 756 - 759]
[Fairhurst, Nathan W. G.; Mahon, Mary F.; Munday, Rachel H.; Carbery, David R. Organic Letters, 2012 , vol. 14, # 3 p. 756 - 759]
[Berhal, Farouk; Takechi, Sho; Kumagai, Naoya; Shibasaki, Masakatsu Chemistry - A European Journal, 2011 , vol. 17, # 6 p. 1915 - 1921]
[Berhal, Farouk; Takechi, Sho; Kumagai, Naoya; Shibasaki, Masakatsu Chemistry - A European Journal, 2011 , vol. 17, # 6 p. 1915 - 1921]
[Berhal, Farouk; Takechi, Sho; Kumagai, Naoya; Shibasaki, Masakatsu Chemistry - A European Journal, 2011 , vol. 17, # 6 p. 1915 - 1921]