Occurrence of piperidine-2,6-dicarboxylic acid (trans) in a red alga, Porphyra tenera.
Author:
Publisher
Japanese Society of Fisheries Science
Subject
Aquatic Science
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Tissues and industrial co-products formed during alginate extraction from Laminaria hyperborea provide different metabolite profiles depending on harvest season;Journal of Applied Phycology;2022-12-27
2. Stereo-Selective Preparation of Teneraic Acid, trans-(2S,6S)-Piperidine-2,6-dicarboxylic Acid, via Anodic Oxidation and Cobalt-Catalyzed Carbonylation;Chemical and Pharmaceutical Bulletin;2017
3. Stereoselective synthesis of piperidine-2,6-dicarboxylic acids by photocatalytic reaction of aqueous cadmium(II) sulfide dispersion;Tetrahedron Letters;1995-05
4. The imine-epoxide rearrangement in the formation of trans-2,6-disubstituted piperidines. A stereoselective synthesis of (±)-teneraic acid;Tetrahedron Letters;1989-01
5. Evolutionary relationships between fungi, red algae, and other simple eucaryotes inferred from total DNA hybridizations to a cloned basidiomycete ribosomal DNA;Experimental Mycology;1986-09
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