389086-08-2Relevant academic research and scientific papers
Studies directed toward the total synthesis of pinnatoxin A: Synthesis of the 6,5,6-dispiroketal (BCD ring) system by double hemiketal formation/hetero-Michael addition strategy
Nakamura, Seiichi,Inagaki, Jun,Kudo, Masashi,Sugimoto, Tomohiro,Obara, Kohei,Nakajima, Makoto,Hashimoto, Shunichi
, p. 10353 - 10374 (2007/10/03)
An efficient, highly stereoselective synthesis of the C10-C26 portion of pinnatoxin A has been achieved, wherein the key step is a highly stereoselective construction of the 6,5,6-dispiroketal (BCD ring) system by an intramolecular hetero-Michael addition of a hemiketal alkoxide reversibly formed under the influence of lithium methoxide.
A Stereoselective synthesis of the C10-C31 (BCDEF ring) portion of pinnatoxin A
Nakamura, Seiichi,Inagaki, Jun,Sugimoto, Tomohiro,Kudo, Masashi,Nakajima, Makoto,Hashimoto, Shunichi
, p. 4075 - 4078 (2007/10/03)
(matrix presented) An efficient synthesis of the C10-C31 (BCDEF ring) portion of pinnatoxin A has been achieved. The key step is a highly stereoselective construction of the dispiroketal (BCD ring) system employing an intramolecular hetero-Michael reaction of a reversibly formed hemiketal alkoxide through the use of LiOMe.
