Stereoselective Synthesis of Protected (2R,3R,4S)-4,7-Diamino-2,3-dihydroxyheptanoic Acid: A Novel Amino Acid of Callipeltins A and D
Author:
Affiliation:
1. School of Chemical and Biological Engineering, Seoul National University, Seoul 151-744, Korea ygkim@snu.ac.kr
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo052676o
Reference36 articles.
1. Photochemical reactivity of aromatic and heteroaromatic nitroderivatives in the presence of arylalkenes
2. Callipeltin A, a Cyclic Depsipeptide Inhibitor of the Cardiac Sodium–Calcium Exchanger and Positive Inotropic Agent
3. Isolation of callipeltins A–C and of two new open-chain derivatives of callipeltin A from the marine sponge Latrunculia sp. A revision of the stereostructure of callipeltins
4. Progress toward the Total Synthesis of Callipeltin A (I): Asymmetric Synthesis of (3S,4R)-3,4-Dimethylglutamine
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1. Stereoselective Synthesis of a Protected Side Chain of Callipeltin A;Organic Letters;2022-09-23
2. Synthesis of the cyclic heptapeptide core of callipeltin A;Organic Chemistry Frontiers;2022
3. Stereoselective Synthesis of (2S,3R)-3-Hydroxyhomoserine Lactone via anti Selective Dihydroxylation of an OBO Group-Protected Vinyl Glycine Analog;APPL CHEM ENG;2020
4. Synthesis of Orthogonally Protected (2R,3R,4S)-4-Amino-2,3-dihydroxyheptane-1,7-dioic Acid;Synthesis;2014-11-06
5. Porifera (Sponges)-5;Encyclopedia of Marine Natural Products;2014-08-07
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