Total synthesis of (.+-.)-eriolanin
โ Scribed by Grieco, Paul A.; Oguri, Tomei; Gilman, S.; DeTitta, George T.
- Book ID
- 126286110
- Publisher
- American Chemical Society
- Year
- 1978
- Tongue
- English
- Weight
- 364 KB
- Volume
- 100
- Category
- Article
- ISSN
- 0002-7863
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๐ SIMILAR VOLUMES
The synthesis of dl-errolantn 1, htghly oxygenated IJO-secoeudesmanollde rsolated from the chloroform extracts of Erronhvllum Forbes (Composltae), as reported , 95% , c MeUNaHITHF, 92% , d CI,CCOCl /Zn-C&thcr/ri,S 5hr ; c ZnlNH,CIIMeOHIOยฐC, 44% from 10 , 1 PhSNa!MeOH/rl, 74% ; g NaBE,/MeOH, quant ,
## Abstract Using a sultone as the key intermediate, the first enantioselective total synthesis of the antileukemic 1,10โ__seco__โeudesmanolides (โ)โeriolanin (**1**) and (โ)โeriolangin (**2**) was achieved, which also established the hitherto unknown absolute configuration of these sesquiterpene l