389085-87-4Relevant academic research and scientific papers
A highly stereoselective synthesis of the C10-C31 (BCDEF ring) portion of pinnatoxin A
Nakamura, Seiichi,Inagaki, Jun,Sugimoto, Tomohiro,Ura, Yasuyuki,Hashimoto, Shunichi
, p. 10375 - 10386 (2007/10/03)
An efficient, highly stereoselective synthesis of the C10-C31 (BCDEF ring) portion of pinnatoxin A has been achieved utilizing tandem double hemiketal formation/intramolecular hetero-Michael addition to construct the 6,5,6-dispiroketal (BCD ring) system a
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.
