✦ LIBER ✦

The conversion of allyl sulfoxides into allyl disulfides via the intramolecular rearrangement of thiosuifoxides

✍ Scribed by Raymond D. Baechler; Sylvia Kourou Daley; Barbara Daly; Kathleen McGlynn

Book ID: 104236921
Publisher: Elsevier Science
Year: 1978
Tongue: French
Weight: 309 KB
Volume: 19
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(01)85055-3

No coin nor oath required. For personal study only.

✦ Synopsis

Sulfoxides are conveniently deomenated by treatment with certain oxygen/sulfur exchange reagents, such as phosphorus pentasulfide, P&C, boron trisulfide, B2S3, and silicon

📜 SIMILAR VOLUMES

Conversion of an Arabinose-Derived Allyl

Conversion of an Arabinose-Derived Allyl Vinyl Ether System into the Functionalized 4-Cycloheptenone via Claisen Rearrangement.

✍ Stefan Juers; Joachim Thiem 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 13 KB

Direct conversion of allylic nitro compo

Direct conversion of allylic nitro compounds into allyl sulphides and allyl sulphones

✍ Ono, Noboru; Hamamoto, Isami; Yanai, Tetsuya; Kaji, Aritsune 📂 Article 📅 1985 🏛 The Royal Society of Chemistry 🌐 English ⚖ 171 KB

Substituent Effect on the Efficiency of

Substituent Effect on the Efficiency of Desulfurizative Rearrangement of Allylic Disulfides

✍ Li, Zhe; Wang, Chen; Fu, Yao; Guo, Qing-Xiang; Liu, Lei 📂 Article 📅 2008 🏛 American Chemical Society 🌐 English ⚖ 769 KB

Efficient stereocontrol in the [2,3] sig

Efficient stereocontrol in the [2,3] sigmatropic rearrangement of allylic sulfoxides

✍ Sato, Tsuneo; Otera, Junzo; Nozaki, Hitosi 📂 Article 📅 1989 🏛 American Chemical Society 🌐 English ⚖ 217 KB

ChemInform Abstract: Synthesis of Neogly

ChemInform Abstract: Synthesis of Neoglycoconjugates by the Desulfurative Rearrangement of Allylic Disulfides.

✍ David Crich; Fan Yang 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 15 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Selectivity in the amination of allylic

Selectivity in the amination of allylic alcohols via intramolecular amidomercuration

✍ Kenn E. Harding; Donald R. Hollingsworth 📂 Article 📅 1988 🏛 Elsevier Science 🌐 French ⚖ 316 KB

This effect would tend to destabrhxe carbocatron character on the 8 carbon and favor nucleoph&c attack at the y-carbon lo This rationale was tested by exammatron of the cychzation reacaons of carbamate 9. Carbamate 9 was prepared from commercrally avarlable as-2-buten-l&ho1 (7). Monoalkylatton of d