✦ LIBER ✦

Applications of N-Phosphinoyloxaziridines in the Conversion of Alkenes to Epoxides and Esters to α-Hydroxyesters.

✍ Scribed by W. Brian Jennings; Adrian Schweppe; Luisa M. Testa; Elena Zaballos-Garcia; Jose Sepulveda-Arques

Publisher: John Wiley and Sons
Year: 2003
Weight: 159 KB
Volume: 34
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200315060

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Dehydration of α-Si

ChemInform Abstract: Dehydration of α-Silylalcohols in the Reductive Conversion of Esters and Ketones into Alkenes.

✍ A. CHENEDE; N. A. RAHMAN; I. FLEMING 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Silphos [PCl3-n(SiO2)n]: A Heterogeneous

Silphos [PCl3-n(SiO2)n]: A Heterogeneous Phosphine Reagent for the Conversion of Epoxides to β-Bromoformates or Alkenes.

✍ Nasser Iranpoor; Habib Firouzabadi; Arezu Jamalian 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 21 KB

Studies on the Base-Promoted Conversion

Studies on the Base-Promoted Conversion of Conjugated Alkynyl Esters to α-Allenyl Esters.

✍ Salvatore D. Lepore; Yuanjun He; Pamela Damisse 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 26 KB

## Abstract For Abstract see ChemInform Abstract in Full Text.

“Syn-Effect” in the Conversion of (E)-α,

“Syn-Effect” in the Conversion of (E)-α,β-Unsaturated Esters to the Corresponding β,γ-Unsaturated Esters.

✍ Samar Kumar Guha; Atsushi Shibayama; Daisuke Abe; Yutaka Ukaji; Katsuhiko Inomat 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 105 KB 👁 1 views

ChemInform Abstract: Silylene Transfer t

ChemInform Abstract: Silylene Transfer to α-Keto Esters and Application to the Synthesis of γ-Lactones.

✍ Brett E. Howard; K. A. Woerpel 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 55 KB

ChemInform Abstract: Ru(III) Catalyzes t

ChemInform Abstract: Ru(III) Catalyzes the Conversion of Epoxides to 1,3-Dioxolanes.

✍ N. IRANPOOR; F. KAZEMI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB

Ru(III) Catalyzes the Conversion of Epoxides to 1,3-Dioxolanes. -Anhydrous RuCl 3 catalyzes the reaction of epoxides with both electron releasing and withdrawing groups with acetone to give 1,3-dioxolanes [cf. (III) and (V)] in good yields. -(IRANPOOR, N.;