Structural and stereochemical diversity in prenylated indole alkaloids containing the bicyclo[2.2.2]diazaoctane ring system from marine and terrestrial fungi-Reference-Cited by-同舟云学术

Structural and stereochemical diversity in prenylated indole alkaloids containing the bicyclo[2.2.2]diazaoctane ring system from marine and terrestrial fungi

Published:2018 Issue:6 Volume:35 Page:532-558
ISSN:0265-0568
Container-title:Natural Product Reports
language:en
Short-container-title:Nat. Prod. Rep.

Author:

Klas Kimberly R.¹²³⁴,Kato Hikaru⁵⁶⁷⁸,Frisvad Jens C.⁹¹⁰¹¹¹²,Yu Fengan¹³¹⁴¹⁵¹⁶⁴,Newmister Sean A.¹³¹⁴¹⁵¹⁶⁴,Fraley Amy E.¹³¹⁴¹⁵¹⁶⁴,Sherman David H.¹³¹⁴¹⁵¹⁶⁴,Tsukamoto Sachiko⁵⁶⁷⁸,Williams Robert M.¹²³⁴¹⁷

Affiliation:

1. Department of Chemistry

2. Colorado State University

3. Fort Collins

4. USA

5. Graduate School of Pharmaceutical Sciences

6. Kumamoto University

7. Kumamoto 862-0973

8. Japan

9. Section for Eukaryotic Biotechnology

10. Departments of System Biology

11. Technical University of Denmark

12. Denmark

13. Life Sciences Institute

14. Departments of Medicinal Chemistry, Chemistry, Microbiology & Immunology

15. The University of Michigan

16. Ann Arbor

17. University of Colorado

Abstract

Various fungi of the generaAspergillus,Penicillium, andMalbrancheaproduce prenylated indole alkaloids possessing a bicyclo[2.2.2]diazaoctane ring system.

Funder

Ministry of Education, Culture, Sports, Science and Technology

Nagase Science Technology Foundation

National Institutes of Health

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/NP/C7NP00042A

Reference144 articles.

1. Studies in relation to biosynthesis—XLII