879873-85-5Relevant academic research and scientific papers
Enantioselective total synthesis of (-)-Clavosolide A and B
Son, Jung Beom,Kim, Si Nae,Kim, Na Yeong,Hwang, Min-Ho,Lee, Wonsun,Lee, Duck Hyung
scheme or table, p. 653 - 663 (2010/08/19)
Enantioselective total synthesis of (-)-clavosolide A and B was reported in full including the synthesis of proposed structure of (-)-clavosoldie A (1), revised structure of (-)-clavosoldie A (5), and revised structure of (-)-clavosoldie B (6). The relative and absolute stereochemistries of the natural products were confirmed unambiguously by comparing the optical rotation values and 1H and 13C NMR spectra of them.
Enantioselective total synthesis of (-)-clavosolide B
Son, Jung Beom,Hwang, Min-Ho,Lee, Wonsun,Lee, Duck-Hyung
, p. 3897 - 3900 (2008/02/11)
Enantioselective synthesis of 2, a revised structure for (-)-clavosolide B, was accomplished by a convergent approach, where syn-selective aldol, hydroxy-directed cyclopropanation, Mitsunobu inversion, Schmidt-type glycosylation, and macrolactonization re
Total synthesis, structural revision, and absolute configuration of (+)-clavosolide A
Son, Jung Beom,Kim, Si Nae,Kim, Na Yeong,Lee, Duck Hyung
, p. 661 - 664 (2007/10/03)
Enantioselective synthesis of 3, a revised structure for clavosolide A, was completed. Both 1H and 13C NMR spectra of the natural and synthetic compounds were identical, and optical rotation measurements identified the absolute confi
