The C(18)-C(24) segment of lasonolide A has been prepared with complete chemodifferentiation of functionality.
Toward the synthesis of tetrodecamycin: asymmetric synthesis of a direct precursor of the C6C18 trans-decalin portion
✍ Scribed by Franz F Paintner; Gerd Bauschke; Kurt Polborn
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 196 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
We report the asymmetric synthesis of a direct precursor of the C6 C18 trans-decalin portion of tetrodecamycin utilising an asymmetric intramolecular Diels-Alder (IMDA) reaction as the key step.
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