ChemInform Abstract: “Tailor-Made” Carbonyl Ylides: (3 + 2) Cycloaddition of the Parent and Optionally Substituted Nonstabilized Carbonyl Ylides.
✍ Scribed by M. HOJO; H. AIHARA; H. ITO; A. HOSOMI
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 34 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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## Abstract 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 v
3 + 2] Cycloaddition of Nonstabilized Azomethine Ylides. Part 7. Stereoselective Synthesis of Epibatidine and Analogues. -The key step in the synthesis of epibatidine (VII) and analogues like (VIII) and (XII) is the stereoselective [3 + 2] cycloaddition of the azomethine ylides (III) and (X). -(
## 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 “Full Text” option. The original article is trackable v