Diversity-oriented synthesis of indole-fused scaffolds and bis(indolyl)methane from tosyl-protected tryptamine-Reference-Cited by-同舟云学术

Diversity-oriented synthesis of indole-fused scaffolds and bis(indolyl)methane from tosyl-protected tryptamine

Published:2024 Issue:14 Volume:22 Page:2824-2834
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wang Liang¹^ORCID,Song Xiaopei¹,Guo Fengxia¹,Xu Lubin¹,Hu Fangzhi¹^ORCID,Guo Feng-Wei¹^ORCID,Li Shuai-Shuai¹^ORCID

Affiliation:

1. College of Chemistry and Pharmaceutical Sciences, Qingdao Agricultural University, Qingdao 266109, China

Abstract

Diversity-oriented synthesis of indole-1,2-fused 1,4-benzodiazepines, tetrahydro-β-carbolines, and 2,2′-bis(indolyl)methanes is presented by control of reaction sites.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB00099D

Reference53 articles.

1. Mushroom-Derived Indole Alkaloids

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4. Indole frameworks via transition-metal-free annulation: a current perspective

5. Recent Advances in Domino Synthesis of Fused Polycyclic N‐Heterocycles Based on Intramolecular Alkyne Hydroamination under Copper Catalysis

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