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The Ester Dienolate [2,3]-Wittig Rearrangement — Development, Opportunities, and Limitations.

✍ Scribed by Martin Hiersemann; Lars Abraham; Annett Pollex

Book ID
101941822
Publisher
John Wiley and Sons
Year
2003
Weight
51 KB
Volume
34
Category
Article
ISSN
0931-7597

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📜 SIMILAR VOLUMES

The ester dienolate [2,3]-Wittig rearran
The ester dienolate [2,3]-Wittig rearrangement. Diastereoselective synthesis of 2,3-dialkenyl-substituted 2-hydroxy-γ-lactones
✍ Martin Hiersemann 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 928 KB

The ester dienolate [2,3]-Wittig rearrangement proceeds with high yield and anti/syn diastereoselection to afford 3-alkoxycarbonyl-3-hydroxy-substituted 1,5-hexadienes. No donor solvent or metal salt additive was necessary to trigger the rearrangement. The rearrangement product was transformed to di

ChemInform Abstract: The Dienolate [2,3]
ChemInform Abstract: The Dienolate [2,3]-Wittig Rearrangement — Diastereoselective Synthesis of Highly Functionalized Tertiary Alcohols.
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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