Reactivity of 1-aminoazetidine-2-carboxylic acid during peptide forming procedures: observation of an unusual variant of the hydrazino turn
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference31 articles.
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1. A Post-Synthetic Modification Strategy for the Preparation of Homooligomers of 3-Amino-1-methylazetidine-3-carboxylic Acid;Synlett;2023-04-11
2. Illuminating the dark conformational space of macrocycles using dominant rotors;Nature Chemistry;2021-02-15
3. Strategic C to N Replacement in β-Peptides: Atomic Level Control of Helical Folding;The Journal of Organic Chemistry;2018-07-02
4. Low-cost and multi-gram scale synthesis of chiral Nβ-Boc protected α-Nα-hydrazino diesters;Tetrahedron Letters;2017-03
5. Intrinsic Folding Proclivities in Cyclic β‐Peptide Building Blocks: Configuration and Heteroatom Effects Analyzed by Conformer‐Selective Spectroscopy and Quantum Chemistry;Chemistry – A European Journal;2015-09-25
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