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Diastereoselective ireland-claisen rearrangement of allylic alcohols

✍ Scribed by Jin K. Cha; S.C. Lewis

Publisher
Elsevier Science
Year
1984
Tongue
French
Weight
260 KB
Volume
25
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis

We are indebted to Professors C. M. Harris. T. M. Harris and D. E. Pearson for thelr assistance wlth HPLC, NMR and CC measurements. respectively.

πŸ“œ SIMILAR VOLUMES

Allyloxy ketone enol ether-claisen rearr
Allyloxy ketone enol ether-claisen rearrangement. regiospecific synthesis of allyl ketones from allyl alcohols
✍ Joseph L.C. Kachinski; Robert G. Salomon πŸ“‚ Article πŸ“… 1977 πŸ› Elsevier Science 🌐 French βš– 212 KB

Claisen rearrangement of ally1 vinyl ethers is an important general method of carboncarbon bond formation for synthesis of y,b-unsaturated aldehydes and ketones. 1 Syntheses of y,b-unsaturated esters and amides are similarly achieved by rearrangements of 2-alkoxy and 2amino-3-oxa-1,5-hexadienes.