✦ LIBER ✦

.alpha.-Arylation of carbonyl groups. Utilization of the p-toluenesulfonylazo olefin functional group as an enolonium synthon

✍ Scribed by Sacks, Clifford E.; Fuchs, P. L.

Book ID: 118152756
Publisher: American Chemical Society
Year: 1975
Tongue: English
Weight: 388 KB
Volume: 97
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja00858a027

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

.alpha.-Arylation of .alpha.,.beta.-unsa

.alpha.-Arylation of .alpha.,.beta.-unsaturated ketones. Utilization of the .alpha.-epoxytosylhydrazone functional group as a .DELTA.2-enonium synthon

✍ Fuchs, Philip L. 📂 Article 📅 1976 🏛 American Chemical Society 🌐 English ⚖ 367 KB

An efficient synthesis of polyoxamic aci

An efficient synthesis of polyoxamic acid utilizing the aryl group as the carboxyl synthon. A new approach to polyhydroxyamino acids

✍ Fumiyoshi Matsuura; Yasumasa Hamada; Takayuki Shioiri 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 327 KB

Abswacr: Polyoxamic acid (1). an amino acid moiety of antifungal antibiotics polyoxins, has been efficiently syntlxsized from Boc-(R)4-hydroxyphenylglycine (3) utilizing its aryl gmup as the carboxy synthon.

Structural effects in solvolytic reactio

Structural effects in solvolytic reactions. 24. Solvolysis of 1-cycloalkyl-1-aryl-1-ethyl p-nitrobenzoates. Effect of .alpha.-cycloalkyl groups in stabilizing an electron-deficient center as revealed by the tool of increasing electron demand

✍ Brown, Herbert C.; Ravindranathan, M.; Rao, C. Gundu 📂 Article 📅 1978 🏛 American Chemical Society 🌐 English ⚖ 516 KB