A Modular Approach for Diversity‐Oriented Synthesis of 1,3‐ <i>trans</i> ‐Disubstituted Tetrahydroisoquinolines: Seven‐Step Asymmetric Synthesis of Michellamines B and C-Reference-Cited by-同舟云学术

A Modular Approach for Diversity‐Oriented Synthesis of 1,3‐ trans ‐Disubstituted Tetrahydroisoquinolines: Seven‐Step Asymmetric Synthesis of Michellamines B and C

Published:2022-06-17 Issue:31 Volume:61 Page:
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew Chem Int Ed

Author:

Bai Miao¹,Jia Shihu¹,Zhang Jingyang¹,Cheng Hong‐Gang¹,Cong Hengjiang¹,Liu Shanshan¹,Huang Zhiqian²,Huang Yaoguo²,Chen Xiaoming²,Zhou Qianghui¹³^ORCID

Affiliation:

1. Sauvage Center for Molecular Sciences Engineering Research Center of Organosilicon Compounds & Materials (Ministry of Education) Hubei Key Lab on Organic and Polymeric Opto-Electronic Materials College of Chemistry and Molecular Sciences and The Institute for Advanced Studies Wuhan University Wuhan 430072 China

2. Daicel Chiral Technologies (China) Co., Ltd. Shanghai 200131 China

3. State Key Laboratory of Bio-Organic and Natural Products Chemistry Shanghai Institute of Organic Chemistry University of Chinese Academy of Sciences 345 Ling Ling Rd Shanghai 200032 China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202205245

Reference99 articles.

2. Naphthylisoquinoline alkaloids potential drug leads

3. Dimeric naphthylisoquinoline alkaloids: polyketide-derived axially chiral bioactive quateraryls

4. Naphthylisoquinoline alkaloids, validated as hit multistage antiplasmodial natural products

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