✦ LIBER ✦

Regio- and stereoselective cyclopentenone annulation by means of ketone-propargyl alcohol adducts

✍ Scribed by Hiyama, Tamejiro; Shinoda, Masaki; Nozaki, Hitosi

Book ID: 127106596
Publisher: American Chemical Society
Year: 1979
Tongue: English
Weight: 293 KB
Volume: 101
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja00500a042

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Regio and stereoselective preparation of

Regio and stereoselective preparation of enolates from ketones by means of sodium bis(trimethylsilyl)-azide

✍ Marcel Gaudemar; Moncef Bellassoued 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 214 KB

The depmtonation of some ketones by sodium bis(trimethylsily1) -azide is regio and stereoselective. The results are different from these observed with LDA.

Regio- and Stereoselective Homocoupling

Regio- and Stereoselective Homocoupling of γ-Arylated tert-Propargyl Alcohols with Liberation of a Ketone Molecule and Successive Cyclization to Produce Fluorescent Dihydrofuran Derivatives.

✍ Atsushi Funayama; Tetsuya Satoh; Masahiro Miura 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 22 KB

## 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, please click on HTML or PDF.

Regio- and Stereoselective Homocoupling

Regio- and Stereoselective Homocoupling of γ-Arylated tert -Propargyl Alcohols with Liberation of a Ketone Molecule and Successive Cyclization To Produce Fluorescent Dihydrofuran Derivatives

✍ Funayama, Atsushi; Satoh, Tetsuya; Miura, Masahiro 📂 Article 📅 2005 🏛 American Chemical Society 🌐 English ⚖ 56 KB