Our interest in the tandem Claisen-ene rearrangement' and the desire to develop efficient methods for the control of both the regio-and stereochemistry of the ene reaction for eventual applications in organic synthesis led us to explore the role of the trimethylsilyl group as a controlling unit. I?
A comparison of substituent field effects on the regiochemistry of the ene reactions of allylic sulfides and ethers
✍ Scribed by Edward L. Clennan; Jaya J. Koola; Ming-Fang Chen
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- French
- Weight
- 848 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
✦ Synopsis
Abstracts
The reactions of 4-methyl-1,2,4-t with allylic ethers aad ftdidea have beea examhd. The diffemt mspowes of the regicchemistty io the two mctio: sea-k4 to changty in the eleetroaic charam of the
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