A convenient new synthesis of homoserine lactone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. A NOVEL SYNTHESIS OF OPTICALLY ACTIVE AZETIDINE-2-CARBOXYLIC ACID
2. Synthesis ofN-t-Boc-L-a-aminoadipic Acid 1-t-Butyl 6-Ethyl Ester from L-Aspartic Acid: A New Route to L-a-Aminoadipic Acid
3. Organocuprates mediated carbon-carbon bond formation in δ position of α-amino esters without racemisation
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1. Dinuclear zinc-catalyzed asymmetric [3 + 2] cyclization reaction for direct assembly of chiral α-amino-γ-butyrolactones bearing three stereocenters;Organic Chemistry Frontiers;2021
2. Synthesis of α-Benzyloxyamino-γ-butyrolactones via a Polar Radical Crossover Cycloaddition Reaction;Organic Letters;2015-12-08
3. A Microwave-Assisted Synthesis of (S)-N-Protected Homoserine γ-Lactones from l-Aspartic Acid;The Journal of Organic Chemistry;2011-07-19
4. Solid-Phase Synthesis of Multiple Classes of Peptidomimetics from Versatile Resin-Bound Aldehyde Intermediates;Journal of the American Chemical Society;2007-05-16
5. Preparation of Difunctional Compounds;Compendium of Organic Synthetic Methods;2006-11-22
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