Synthesis of the Carboline Disaccharide Domain of Shishijimicin A-Reference-Cited by-同舟云学术

Synthesis of the Carboline Disaccharide Domain of Shishijimicin A

Published:2011-06-28 Issue:15 Volume:13 Page:3924-3927
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Nicolaou K. C.¹,Kiappes J. L.¹,Tian Weiwei¹,Gondi Vijaya B.¹,Becker Jochen¹

Affiliation:

1. Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States, and The Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol201444t

Reference30 articles.

1. Chemistry and Biology of the Enediyne Anticancer Antibiotics

2. The Enediyne Antibiotics

3. The chemistry of enediynes, enyne allenes and related compounds

4. Understanding and Exploiting Natures Chemical Arsenal: The Past,Present and Future of Calicheamicin Research

5. Designed Enediyne Antitumor Agents

Cited by 22 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. Thioacetalation and Multi-Component Thiomethylative Friedel-Crafts Arylation Using BF₃SMe₂;ACS Omega;2023-01-19

2. A Direct and an Efficient Regioselective Synthesis of 1,2-Benzothiazine 1,1-dioxides, β-Carbolinones, Indolo[2,3-c]pyran-1-ones, Indolo[3,2-c]pyran-1-ones, Thieno[2,3-c]pyran-7-ones and Pyrano[3’,4’:4,5]imidazo[1,2-a]pyridin-1-ones via Tandem Stille/Heterocyclization Reaction;Molecules;2020-11-04

3. A Mild Bischler–Napieralski-Type Cyclization of Trichloromethyl Carbamates for the Synthesis of β-Carbolinones;HETEROCYCLES;2020

4. Pd/Cu Cocatalyzed Oxidative Tandem C–H Aminocarbonylation and Dehydrogenation of Tryptamines: Synthesis of Carbolinones;The Journal of Organic Chemistry;2019-02-22

5. An overview on synthetic entries to tetrahydro-β-carbolines;Tetrahedron;2019-02