An efficient synthesis method targeted to marine alkaloids marinacarbolines A–D and their antitumor activities-Reference-Cited by-同舟云学术

An efficient synthesis method targeted to marine alkaloids marinacarbolines A–D and their antitumor activities

Published:2015-01-28 Issue:3 Volume:17 Page:299-305
ISSN:1028-6020
Container-title:Journal of Asian Natural Products Research
language:en
Short-container-title:Journal of Asian Natural Products Research

Author:

Li Jun,Tang Yang,Jin Hui-Juan,Cui Yi-Di,Zhang Li-Juan,Jiang Tao

Publisher

Informa UK Limited

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,General Medicine,Analytical Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/10256018808623883

Reference12 articles.

1. β-Carboline Alkaloids: Biochemical and Pharmacological Functions

2. Room-Temperature Aromatization of Tetrahydro-β-carbolines by 2-Iodoxybenzoic Acid: Utility in a Total Synthesis of Eudistomin U

3. Discovery of McbB, an Enzyme Catalyzing the β-Carboline Skeleton Construction in the Marinacarboline Biosynthetic Pathway

4. Antimalarial β-Carboline and Indolactam Alkaloids from Marinactinospora thermotolerans, a Deep Sea Isolate

5. First Total Syntheses of 1,3-Disubstituted β-Carboline Alkaloids, Dichotomide I and Marinacarbolines A-D

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