Brasiliquinone B (2) was synthesized from 7-methoxy-l-tetralone in 8 steps making use of Friedel-Crafts alkylation as a key step.
First total synthesis of (±)-adunctin B
✍ Scribed by Kenji Arimitsu; Sayo Nomura; Hiroki Iwasaki; Minoru Ozeki; Masayuki Yamashita
- Book ID
- 113930119
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- French
- Weight
- 255 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A general approach to the synthesis of all known strobilurins -a class of natural products -is outlined with strobilurin B as an example. Strobilurin A (1) was first isolated in 1969 under the name of mucidin by Musilek and co-workers 1) from the fungus Oudemansiella mucida. The structure as well a
Total synthesis of theopederin B, isolated from marine sponge, was accomplished by coupling pederic acid, as the left half, with trioxodecaline amine as the right half. Key reactions for synthesizing the amine were SmI 2 -promoted Reformatsky reaction, stereoselective allylation followed by Sharples
## Abstract For Abstract see ChemInform Abstract in Full Text.
## 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, please click on HTML or PDF.
## 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, please click on HTML or PDF.