✦ LIBER ✦

Catalysts Based on Amino Acids for Asymmetric Reactions in Water

✍ Scribed by Joanna Paradowska; Maciej Stodulski; Jacek Mlynarski

Publisher: John Wiley and Sons
Year: 2009
Tongue: English
Weight: 448 KB
Volume: 48
Category: Article
ISSN: 0044-8249
DOI: 10.1002/anie.200802038

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Catalysts Based on

ChemInform Abstract: Catalysts Based on Amino Acids for Asymmetric Reactions in Water

✍ Joanna Paradowska; Maciej Stodulski; Jacek Mlynarski 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 11 KB 👁 2 views

Enantioselective β-Amino Acid Synthesis

Enantioselective β-Amino Acid Synthesis Based on Catalyzed Asymmetric Acyl Halide – Aldehyde Cyclocondensation Reactions

✍ Scott G. Nelson; Keith L. Spencer 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 87 KB 👁 1 views

Enantioselective β-Amino Acid Synthesis

Enantioselective β-Amino Acid Synthesis Based on Catalyzed Asymmetric Acyl Halide – Aldehyde Cyclocondensation Reactions

✍ Scott G. Nelson; Keith L. Spencer 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 87 KB 👁 1 views

Synthesis of a Biphenyl-Based Axially Ch

Synthesis of a Biphenyl-Based Axially Chiral Amino Acid as a Highly Efficient Catalyst for the Direct Asymmetric Aldol Reaction.

✍ Taichi Kano; Osamu Tokuda; Keiji Maruoka 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

Amphiphilic Polymer Supports for the Asy

Amphiphilic Polymer Supports for the Asymmetric Hydrogenation of Amino Acid Precursors in Water

✍ M. Tobias Zarka; Oskar Nuyken; Ralf Weberskirch 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 168 KB 👁 2 views

Enhanced Activity and Stereoselectivity

Enhanced Activity and Stereoselectivity of Polystyrene-Supported Proline-Based Organic Catalysts for Direct Asymmetric Aldol Reaction in Water

✍ Michelangelo Gruttadauria; Anna Maria Pia Salvo; Francesco Giacalone; Paola Agri 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 580 KB

## Abstract Several polystyrene‐supported proline dipeptides and a prolinamide derivative were prepared by thiol–ene coupling. These materials were used as catalysts for the direct asymmetric aldol reaction in water, and results compared with unsupported catalysts in water. Such an approach gave mo