✦ LIBER ✦

Vinylic cations from solvolysis. IX. Trifluoroacetolysis of 1-anisyl-2-methylpropen-1-yl arylsulfonates

✍ Scribed by Zvi Rappoport; Joseph Kaspi

Book ID: 104248258
Publisher: Elsevier Science
Year: 1971
Tongue: French
Weight: 245 KB
Volume: 12
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(01)97355-1

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Vinylic cations from solvolysis. XXIII.

Vinylic cations from solvolysis. XXIII. Degenerate .beta.-anisyl rearrangement during the solvolysis of 2-anisyl-1,2-diphenylvinyl bromides. Free ions as intermediates

✍ Rappoport, Zvi; Noy, Etta; Houminer, Yoram 📂 Article 📅 1976 🏛 American Chemical Society 🌐 English ⚖ 865 KB

Vinyl cations, 22 a 1,2-hydride shift in

Vinyl cations, 22 a 1,2-hydride shift in the solvolysis of 3-methyl-1-buten-2-yl triflate

✍ Klaus-Peter Jäckel; Michael Hanack 📂 Article 📅 1975 🏛 Elsevier Science 🌐 French ⚖ 137 KB

Recently we reprted about the first example of a 1.2-hydride shift durmg the generation of a vrnyl cation, a process well known for trlsubstituted car&mum ions 2) :Thls was obsermildurlng the solvolys~s of cls-and trans-3-cyclop~l-2-propen-2-yl-trifl~~~esulfo~~(tnflate)3! --The 1.2-hydride shLft was

Triple Bond Participation and a Bent Vin

Triple Bond Participation and a Bent Vinyl Cation in the Trifluoroacetolysis of 6-Heptyn-2-yl p-Toluenesulfonate 1

✍ Peterson, Paul E.; Kamat, Rajaninath J. 📂 Article 📅 1966 🏛 American Chemical Society 🌐 English ⚖ 274 KB