✦ LIBER ✦

Stereochemical fate of an asymmetric migrating group in the pinacol rearrangement

✍ Scribed by Beggs, J. J.; Meyers, M. B.

Book ID: 121379424
Publisher: Royal Society of Chemistry
Year: 1970
Weight: 671 KB
Category: Article
ISSN: 0045-6470
DOI: 10.1039/J29700000930

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Intrinsic migration aptitudes of alkyl g

Intrinsic migration aptitudes of alkyl groups in a pinacol rearrangement

✍ Eckehardt Wistuba; Christoph Rüchardt 📂 Article 📅 1981 🏛 Elsevier Science 🌐 French ⚖ 201 KB

Stereospecificity of Hydrogen Migration

Stereospecificity of Hydrogen Migration in the Pinacol Rearrangement

✍ Mislow, Kurt; Siegel, Maurice 📂 Article 📅 1952 🏛 American Chemical Society 🌐 English ⚖ 288 KB

THE PINACOL-PINACOLIN REARRANGEMENT. THE

THE PINACOL-PINACOLIN REARRANGEMENT. THE RELATIVE MIGRATION APTITUDES OF ARYL GROUPS 1

✍ Bachmann, W. E.; Moser, Frank H. 📂 Article 📅 1932 🏛 American Chemical Society 🌐 English ⚖ 681 KB

The Stereochemical Fate of the Cycloprop

The Stereochemical Fate of the Cyclopropyl Ring in the Vinylcyclopropane Rearrangement

✍ Willcott, M. Robert.; Cargle, Virgil H. 📂 Article 📅 1967 🏛 American Chemical Society 🌐 English ⚖ 294 KB

Rearrangement of Alkyl Groups. Kinetic a

Rearrangement of Alkyl Groups. Kinetic and Tracer Studies in the Pinacol Rearrangement 1

✍ Stiles, Martin; Mayer, Raymond P. 📂 Article 📅 1959 🏛 American Chemical Society 🌐 English ⚖ 938 KB

Completely stereospecific 1,2-migration

Completely stereospecific 1,2-migration of alkyl groups in Et2AlCl promoted pinacol-type rearrangement

✍ Gen-ichi Tsuchihashi; Katsuhiko Tomooka; Keisuke Suzuki 📂 Article 📅 1984 🏛 Elsevier Science 🌐 French ⚖ 257 KB

## swnmary: Completely stereospecific 1,2-migration of alkyl groups was achieved in Et2AlCL- prowted pinacoZ-type rearrangement of chiral B-mesyZoxy alcohols to give optically pure aalkyl ketones including both enantiomers of 4-methyl-3-hexanone, an alarm pheromone of ant.