The use of two-dimensional long-range δC/δH correlation in conjunction with the one-dimensional proton-coupled 13C NMR spectrum in the structural elucidation of ekeberginine, a new carbazole alkaloid from (meliaceae)
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Techniques for Signal Assignment in13C-NMR Spectroscopy of Naturally Occurring Aromatic Compounds
2. Structure elucidation of phomopsin A, a novel cyclic hexapeptide mycotoxin produced by Phomopsis leptostromiformis
3. Application of long range j c-h resolved 2d spectroscopy (lrjr) in structural elucidation of natural products. The structure of oxirapentyn
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1. Senegalin, a new phenylpropanoid and other secondary metabolites from the stem bark of Ekebergia senegalensis A. Juss. (Meliaceae);Natural Product Research;2020-02-24
2. Phytocarbazoles: alkaloids with great structural diversity and pronounced biological activities;Phytochemistry Reviews;2017-07-07
3. Short synthesis of carbazole alkaloids: Ekeberginine, murrayaquinone A, and glycozoline;Synthetic Communications;2016-07-29
4. Total Synthesis of Carbazole Alkaloids - Ekeberginine, Harmandianamine A, and Furanoclausamine B;European Journal of Organic Chemistry;2014-01-15
5. Transition metals in organic synthesis. Part 108: first total synthesis of ekeberginine;Tetrahedron Letters;2013-02
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