Introduction 2 Fermentation and Isolation 3 Structure Determination 4 Biosynthesis 5 Metabolism 6 Chemistry 6.1 Total Synthesis 6.2 Partial Synthesis 6.3 The Interconversion of the Avermectins and Mil bemycins 6.4 Protection and Acylation 6.5 Oxidations 6.6 Alkylation 6.7 Reduction 6.8 Avermectin Aglycons and their Monosaccharide Analogues 7 Structure-Activity Relationships 8 Conclusion 9 References* Wherever avermectins are described in this Report by using only the first two identifying characters, as in A2, this refers to mixtures of the a and b analogues. In these cases, only the structure of the major component is indicated in the diagram. Where fully identified, as in B2b, this implies the use of pure compound.
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.