A concise total synthesis of sespenine, a structurally unusual indole terpenoid from Streptomyces-Reference-Cited by-同舟云学术

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A concise total synthesis of sespenine, a structurally unusual indole terpenoid from Streptomyces

Published:2016 Issue:3 Volume:3 Page:368-374
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Sun Yu¹²³⁴⁵,Meng Zhanchao¹²³⁴⁵,Chen Pengxi¹²³⁴⁵,Zhang Deliang¹²³⁴⁵,Baunach Martin⁶⁷⁸⁹,Hertweck Christian⁶⁷⁸⁹,Li Ang¹²³⁴⁵

Affiliation:

1. State Key Laboratory of Bioorganic and Natural Products Chemistry

2. Collaborative Innovation Center of Chemistry for Life Sciences

3. Shanghai Institute of Organic Chemistry

4. Chinese Academy of Sciences

5. Shanghai 200032

6. Leibniz Institute for Natural Product Research and Infection Biology

7. HKI

8. Jena

9. Germany

Abstract

A ten-step (the longest linear sequence) total synthesis of sespenine was accomplished.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/QO/C5QO00416K

Reference143 articles.

1. Synthetic studies of marine alkaloids hapalindoles. Part I Total synthesis of (±)-hapalindoles J and M

2. Synthetic studies of marine alkaloids hapalindoles. Part 3 Total synthesis of (±)-hapalindoles H and U

3. Synthesis and absolute configuration of (+)-hapalindole Q

4. Stereocontrolled Synthesis of (-)-Hapalindole G

5. Preparation of Alkyl-Substituted Indoles in the Benzene Portion. Part 12. Enantiospecific Synthesis of Hapalindole O.

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