Role of Secondary Structure in the Asymmetric Acylation Reaction Catalyzed by Peptides Based on Chiral Cα-Tetrasubstituted α-Amino Acids-Reference-Cited by-同舟云学术

Role of Secondary Structure in the Asymmetric Acylation Reaction Catalyzed by Peptides Based on Chiral Cα-Tetrasubstituted α-Amino Acids

Published:2004-05-01 Issue:11 Volume:69 Page:3849-3856
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Formaggio Fernando¹,Barazza Alessandra¹,Bertocco Andrea¹,Toniolo Claudio¹,Broxterman Quirinus B.¹,Kaptein Bernard¹,Brasola Elena¹,Pengo Paolo¹,Pasquato Lucia¹,Scrimin Paolo¹

Affiliation:

1. Department of Chemistry, University of Padova, and ICB, CNR, 35131 Padova, Italy, DSM Pharma Chemicals, Advanced Synthesis and Catalysis, P.O. Box 18, 6160 MD Geleen, The Netherlands, and Department of Chemistry, University of Padova, and ITM, CNR, 35131 Padova, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo040107v

Reference51 articles.

1. Combinatorial catalysis: identification of potent chiral catalysts through fluorescent bead signaling

2. Amino acids and peptides as asymmetric organocatalysts

3. Minimal Acylase-Like Peptides. Conformational Control of Absolute Stereospecificity

4. A Chemosensor-Based Approach to Catalyst Discovery in Solution and on Solid Support

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