Multi-functionalized chiral crown ethers as enzyme models for the synthesis of peptides. Multiple chiral recognition in the enzyme model
- 1 April 1989
- journal article
- research article
- Published by Springer Nature in Journal of inclusion phenomena and molecular recognition in chemistry
- Vol. 7 (2) , 267-276
- https://doi.org/10.1007/bf01060727
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Functionalized crown ethers as an approach to the enzyme model for the synthesis of peptidesJournal of the American Chemical Society, 1985
- Approaches to the synthesis of enzyme model systems. Regioselective transacylation reactions between thiol-containing crown ethers and amino acid ester saltsTetrahedron Letters, 1978
- A Macrocyclic Enzyme Model System. An Electrostatic-Hydrophobic Double-Field Catalysis by a [20]Paracyclophane in the Deacylation of p-Nitrophenyl HexadecanoateBulletin of the Chemical Society of Japan, 1976
- Synthetic simulation of nonribosomal peptide biosynthesis. A dual role of alkylthiol esters in peptide synthesisCellular and Molecular Life Sciences, 1976