✦ LIBER ✦

Intermolecular asymmetric Heck reactions with 2,2-diethyl-2,3-dihydrofuran

✍ Scribed by Alan J Hennessy; David J Connolly; Yvonne M Malone; Patrick J Guiry

Publisher: Elsevier Science
Year: 2000
Tongue: French
Weight: 72 KB
Volume: 41
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)01325-3

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Intermolecular Asym

ChemInform Abstract: Intermolecular Asymmetric Heck Reactions with 2,2-Diethyl-2,3-dihydrofuran.

✍ Alan J. Hennessy; David J. Connolly; Yvonne M. Malone; Patrick J. Guiry 📂 Article 📅 2000 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

From 2,3-dihydrofuran to 2,2-dialkyl-2,3

From 2,3-dihydrofuran to 2,2-dialkyl-2,3-dihydrofurans: new substrates for the intermolecular asymmetric Heck reaction

✍ Tim G Kilroy; Alan J Hennessy; David J Connolly; Yvonne M Malone; Annette Farrel 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 229 KB

ChemInform Abstract: 2,2-Dimethyl-2,3-di

ChemInform Abstract: 2,2-Dimethyl-2,3-dihydrofuran, a New Substrate for Intermolecular Asymmetric Heck Reactions.

✍ Alan J. Hennessy; Yvonne M. Malone; Patrick J. Guiry 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

The Application of HETPHOX Ligands to th

The Application of HETPHOX Ligands to the Asymmetric Intermolecular Heck Reaction of 2,3-Dihydrofuran and 2,2-Disubstituted-2,3-dihydrofurans

✍ Tim G. Kilroy; Pier Giorgio Cozzi; Nicole End; Patrick J. Guiry 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 7 KB 👁 3 views

Enantio- and Regioselective Heck-Type Re

Enantio- and Regioselective Heck-Type Reaction of Arylboronic Acids with 2,3-Dihydrofuran.

✍ Liza Penn; Alina Shpruhman; Dmitri Gelman 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 25 KB 👁 1 views

The asymmetric cyclohexenylation of 2,2-

The asymmetric cyclohexenylation of 2,2-dimethyl-2,3-dihydrofuran

✍ Alan J Hennessy; Yvonne M Malone; Patrick J Guiry 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 154 KB

The palladium catalysed asymmetric cyclohexenylation of 2,2-dimethyl-2,3-dihydrofuran is described. Use of this substrate allowed for an easy and direct comparison of a range of ligands in this reaction. The ligands employed included BINAP and phosphinamines and enantioselectivities of up to 97% wer