Absfracfi Avemectin B la A44,4a ,2, has been obtained from avenneztin B la. 1, and its bioactivity evaluated. The key step of the transfommtion is the reduction of an intemxdiate allylic radical with aBu@nH. The avermectins are disaccharide derivatives of a structurally similar group of pentacyclic
Synthesis of a C16–C28 spiroacetal fragment of avermectin B1a and reassignment of some 1H and 13C resonances of avermectin B1a
✍ Scribed by David Diez-Martin; Peter Grice; Hartmuth C. Kolb; Steven V. Ley; Andrew Madin
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- French
- Weight
- 235 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A new method for the synthesis of unsaturated spiroacetals from 2-benzenesulphonyltetmhydropyrans is presented IH and 13C studies of one of these spiroacetals led to a reassignment of some 1H and 13C resonances of Avermectin B la.
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## Abstract A unique and practical synthetic sequence for rapid access to polyketides and to further the spiroacetals derived from them, which utilizes a bidirectional Hosomi–Sakurai allylation approach around key allylsilanes in the synthesis of the AB and CD ring systems of spongistatin 1 and 2,