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Tripeptides as Efficient Asymmetric Catalysts for 1,4-Addition Reactions of Aldehydes to Nitroolefins–A Rational Approach

✍ Scribed by Markus Wiesner; Jefferson D. Revell; Helma Wennemers

Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
384 KB
Volume
120
Category
Article
ISSN
0044-8249

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📜 SIMILAR VOLUMES

ChemInform Abstract: Tripeptides as Effi
ChemInform Abstract: Tripeptides as Efficient Asymmetric Catalysts for 1,4-Addition Reactions of Aldehydes to Nitroolefins — A Rational Approach.
✍ Markus Wiesner; Jefferson D. Revell; Helma Wennemers 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 55 KB 👁 2 views

## 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 of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Tripeptides of the Type H-D-Pro-Pro-Xaa-
Tripeptides of the Type H-D-Pro-Pro-Xaa-NH2 as Catalysts for Asymmetric 1,4-Addition Reactions: Structural Requirements for High Catalytic Efficiency
✍ Markus Wiesner; Markus Neuburger; Helma Wennemers 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 326 KB

## Abstract Analysis of the structural and functional requirements within the asymmetric peptidic catalyst H‐D‐Pro‐Pro‐Asp‐NH~2~ led to the development of the closely related peptide H‐D‐Pro‐Pro‐Glu‐NH~2~ as an even more efficient catalyst for asymmetric conjugate addition reactions of aldehydes to