The sesquiterpene lactone yomogin k), isolated from Artemisia princeps Pamp. by Geismann,' contains a cross-conjugated dienone system of the a-santonin type as well as an a-methylene-ybutyrolactone grouping. Since dienones related to a-santonin readily undergo photochemical rearrangements into hydro
โฆ LIBER โฆ
Total synthesis of dl-3-oxodiplophyllin and dl-yomogin
โ Scribed by Caine, Drury; Hasenhuettl, Gerard
- Book ID
- 126116671
- Publisher
- American Chemical Society
- Year
- 1980
- Tongue
- English
- Weight
- 616 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
The total synthesis of dl-yomogin
โ
Drury Caine; Gerard Hasenhuettl
๐
Article
๐
1975
๐
Elsevier Science
๐
French
โ 182 KB
Total synthesis of dl-elaeocarpine and d
โ
Tadasu Tanaka; Ikuo Iijima
๐
Article
๐
1970
๐
Elsevier Science
๐
French
โ 220 KB
Total Synthesis of dl -Veatchine and dl
โ
Nagata, Wataru.; Narisada, Masayuki.; Wakabayashi, Toshio.; Sugasawa, Tsutomu.
๐
Article
๐
1967
๐
American Chemical Society
๐
English
โ 823 KB
Total Synthesis of dl -Garryine and dl -
โ
Nagata, Wataru.; Narisada, Masayuki.; Wakabayashi, Toshio.; Sugasawa, Tsutomu.
๐
Article
๐
1964
๐
American Chemical Society
๐
English
โ 274 KB
Total synthesis of dl-cedrene and dl-ced
โ
Corey, Elias J.; Girotra, Narindar N.; Mathew, C. Thomas
๐
Article
๐
1969
๐
American Chemical Society
๐
English
โ 321 KB
The synthesis of 3-spirooxindole derivat
โ
Yoshio Ban; Naomasa Taga; Takeshi Oishi
๐
Article
๐
1974
๐
Elsevier Science
๐
French
โ 245 KB
After we published the intramolecular cyclization of the oxindole iminoether,l Scott made a proposal claiming an important role of the oxindole alkaloid in the biosynthesis of various indole alkaloids. 2 Thus, attention was drawn to synthesize the pentacyclic oxindole alkaloids which are abundant in