𝔖 Bobbio Scriptorium
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The dianion Claisen rearrangement of β-hydroxy esters

✍ Scribed by Mark J. Kurth; Chan-Mo Yu


Book ID
104242294
Publisher
Elsevier Science
Year
1984
Tongue
French
Weight
239 KB
Volume
25
Category
Article
ISSN
0040-4039

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✦ Synopsis


CZaisen rearrwngement of B-hydroxy atlytic ester dianions povides stereocontrotted access to three contiguous chira2 centers on an acyctic frwnework; ax wuzmbiguous method has been devetoped for assessing dtistereosetectivity.


📜 SIMILAR VOLUMES


Claisen rearrangement of allyl esters
✍ Ireland, Robert E.; Mueller, Richard H. 📂 Article 📅 1972 🏛 American Chemical Society 🌐 English ⚖ 233 KB
Enolate claisen rearrangement of glycola
✍ James Kallmerten; Thomas J. Gould 📂 Article 📅 1983 🏛 Elsevier Science 🌐 French ⚖ 251 KB

The enolate Claisen rearrangement of O-protected allylic glycolates yields functionalized acyclic systems with high syn and anti stereoselectivity. step in a short synthesis of threz-methylheptan-3-ol, This procedure is the key an aggregation pheromone of the European elm bark beetle.

Claisen-Haase rearrangement of enol este
✍ F. Gogan; A.E. O'Briain; E.M. Philbin; N.S. O'Connor; R.F. Timoney; T.S. Wheeler 📂 Article 📅 1958 🏛 Elsevier Science 🌐 French ⚖ 313 KB