A stereospecific sequence from the allylic alcohol 3 to the new anti-biotic, cycloeudesmol 2, in 9 steps (21.7% overall yield) is described.
A stereospecific total synthesis of waburganal
β Scribed by David J. Goldsmith; Hollis S. Kezar III
- Publisher
- Elsevier Science
- Year
- 1980
- Tongue
- French
- Weight
- 190 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0040-4039
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
A stereospecific sequence from the octalindlone 2 leads In 21 steps to the new lnsecttcrde ajuqarin-IV. Formation of the butenohde portion is conveniently achteved from acid 21 by successive use of the reaqents trts(tr~methylsiloxy)ethylene and ketenyhdenetrtphenyl-phosphorane.