✦ LIBER ✦

1,3-Shifts. II. The Stereochemistry of the Rearrangement of α-Alkoxystyrenes 1

✍ Scribed by Wiberg, Kenneth B.; Rowland, Bertram I.

Book ID: 126849930
Publisher: American Chemical Society
Year: 1955
Tongue: English
Weight: 656 KB
Volume: 77
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja01610a023

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

1,3-Shifts. VI. The Kinetics of the Rear

1,3-Shifts. VI. The Kinetics of the Rearrangement of α-Benzyloxystyrene

✍ Wiberg, Kenneth B.; Roy Kintner, R.; Motell, Edwin L. 📂 Article 📅 1963 🏛 American Chemical Society 🌐 English ⚖ 690 KB

1,3-Shifts. IV. The Kinetics of the Ther

1,3-Shifts. IV. The Kinetics of the Thermal Rearrangement of α-Phenethyl Chlorocarbonates 1

✍ Wiberg, Kenneth B.; Shryne, Thomas M. 📂 Article 📅 1955 🏛 American Chemical Society 🌐 English ⚖ 602 KB

The Stereochemistry of Aromatic Alkylati

The Stereochemistry of Aromatic Alkylations. II. The Thermal Rearrangement of Alkyl Aryl Ethers 1

✍ Hart, Harold; Eleuterio, Herbert S. 📂 Article 📅 1954 🏛 American Chemical Society 🌐 English ⚖ 516 KB

1,3-Shifts. III. The Kinetics of the The

1,3-Shifts. III. The Kinetics of the Thermal Rearrangement of Phenyl Benzanilimino Ethers 1

✍ Wiberg, Kenneth B.; Rowland, Bertram I. 📂 Article 📅 1955 🏛 American Chemical Society 🌐 English ⚖ 551 KB

Stereochemistry of the 1,2-Wittig rearra

Stereochemistry of the 1,2-Wittig rearrangement: A synthesis of syn-1,3-diol monoethers

✍ Stuart L. Schreiber; Mark T. Goulet 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 259 KB

The [1,2] Wittig rearrangement of P-alkoxyalkyl ally1 ethers has been studied and found to provide syn-1,3-diol derivatives in 14-32% yield and with useful levels of diastereoselection. The rearrangement of a-metalated ethers (Wittig rearrangement) has been of interest to investigators since its di

The Rearrangement of α,α'-Dibromoketones

The Rearrangement of α,α'-Dibromoketones 1

✍ Wagner, R. B.; Moore, James A. 📂 Article 📅 1950 🏛 American Chemical Society 🌐 English ⚖ 496 KB