Enantioselective intramolecular Pictet–Spengler type annulation of indole-linked 3-methyleneisoindolin-1-ones-Reference-Cited by-同舟云学术

Enantioselective intramolecular Pictet–Spengler type annulation of indole-linked 3-methyleneisoindolin-1-ones

Published:2022 Issue:20 Volume:46 Page:9582-9586
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Liu Min¹²³,Li Wenzhe¹²³,Huang Min¹²³,Yan Yingkun¹²³,Li Min¹²³,Cao Lianyi¹²³,Zhang Xiaomei¹²³^ORCID

Affiliation:

1. Asymmetric Synthesis and Chiraltechnology Key Laboratory of Sichuan Province, Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu, China

2. Department of Chemistry, Xihua University, Chengdu, China

3. University of Chinese Academy of Sciences, Beijing, China

Abstract

Asymmetric intramolecular Pictet–Spengler type annulation of indole-linked 3-methyleneisoindolin-1-ones provided isoindolinone fused tetrahydro β-carbolines with moderate to good enantioselectivities.

Funder

National Natural Science Foundation of China

Xihua University

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D2NJ00517D

Reference59 articles.

1. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit

2. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit