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Claisen-Haase rearrangement of enol esters

โœ Scribed by F. Gogan; A.E. O'Briain; E.M. Philbin; N.S. O'Connor; R.F. Timoney; T.S. Wheeler

Publisher
Elsevier Science
Year
1958
Tongue
French
Weight
313 KB
Volume
3
Category
Article
ISSN
0040-4020

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๐Ÿ“œ SIMILAR VOLUMES

Enolate claisen rearrangement of glycola
Enolate claisen rearrangement of glycolate esters
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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.

Ester enolate Claisen rearrangement usin
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Polystyrene-diethylsilane resin (PS-DES) was treated with triflic acid to form a highly reactive polymer silyl triflate. The silyl triflate reacted with enolizable allylic esters in the presence of Et3N to afford resin-bound silyl ketene acetals, which undergo Ireland-Claisen rearrangement at elevat