Synthesis of all isomers of pulcherrimine, a bitter principle in the sea urchin ovary
Author:
Funder
Japan Science and Technology Corporation
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Isolation and Structure of Pulcherrimine, a Novel Bitter-Tasting Amino Acid, from the Sea Urchin (Hemicentrotus pulcherrimus) Ovaries
2. Synthesis of cis-4-(phosphonooxy)-2-piperidinecarboxylic acid, an N-methyl-D-aspartate antagonist
3. Practical, Stereoselective Synthesis of Palinavir, a Potent HIV Protease Inhibitor
4. Enantioselective Synthesis of (2R,4S)- and (2S,4R)-4-Hydroxypipecolic Acid from d-Glucoheptono-1,4-lactone
5. Asymmetric synthesis of cis-(−)-(2R4S)-4-(phosphonomethyl)-2-piperidinecarboxylic acid, a potent NMDA receptor antagonist
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1. Extension of immature stage of Hemicentrotus pulcherrimus ovary for reduction of the bitter compound (pulcherrimine) by water temperature manipulation;Fisheries Science;2023-07-31
2. Echinoderms;Encyclopedia of Marine Natural Products;2014-08-07
3. ChemInform Abstract: Synthesis of All Isomers of Pulcherrimine, a Bitter Principle in the Sea Urchin Ovary.;ChemInform;2010-05-22
4. Effect of Season on the Sensory Quality of Sea Urchin (Evechinus chloroticus) Roe;Journal of Food Science;2010-01
5. Grubbs’ Ruthenium-Carbenes Beyond the Metathesis Reaction: Less Conventional Non-Metathetic Utility;Chemical Reviews;2009-07-02
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