✦ LIBER ✦

A Ligand Structure–Activity Study of DNA-Based Catalytic Asymmetric Hydration and Diels–Alder Reactions.

✍ Scribed by Fiora Rosati; Dr. Gerard Roelfes

Book ID: 112019026
Publisher: John Wiley and Sons
Year: 2011
Tongue: English
Weight: 242 KB
Volume: 3
Category: Article
ISSN: 1867-3880
DOI: 10.1002/cctc.201000440

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

α,β-Unsaturated 2-Acyl Imidazoles as a P

α,β-Unsaturated 2-Acyl Imidazoles as a Practical Class of Dienophiles for the DNA-Based Catalytic Asymmetric Diels−Alder Reaction in Water

✍ Feringa, Ben L.; Roelfes, Gerard; Boersma, Arnold J. 📂 Article 📅 2007 🏛 American Chemical Society 🌐 English ⚖ 108 KB

Asymmetric Diels-Alder reactions catalyz

Asymmetric Diels-Alder reactions catalyzed by chiral lanthanide(III) trifluoromethanesulfonates. Unique structure of the triflate and stereoselective synthesis of both enantiomers using a single chiral source and a choice of achiral ligands

✍ Shū Kobayashi; Haruro Ishitani; Iwao Hachiya; Mitsuharu Araki 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 868 KB

Chiral lanthanide trifluoromethanesulfonates (triflates) were developed and the unique structure of the triflates was revealed. In the presence of a catalytic amount of the triflate, acyl-2,3-oxazolidin-2-ones reacted with cyclopentadiene to afford the Diels-Alder adducts in high yields and with hi