An efficient method for 3, 4‐dihydroisoquinolinium ion formation, leading to a facile introduction of nucleophiles-Reference-Cited by-同舟云学术

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An efficient method for 3, 4‐dihydroisoquinolinium ion formation, leading to a facile introduction of nucleophiles

Published:2020-12-22 Issue:3 Volume:58 Page:751-756
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:J Heterocyclic Chem

Author:

Shimizu Makoto¹²^ORCID,Kawamura Takato²,Fukumoto Shinya²,Mizota Isao²,Zhu Yusong¹

Affiliation:

1. School of Energy Science and Engineering Nanjing Tech University Nanjing China

2. Department of Chemistry for Materials, Graduate School of Engineering Mie University Tsu Japan

Funder

Japan Society for the Promotion of Science

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Wiley

Subject

Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.4211

Reference36 articles.

1. Enzyme catalysed Pictet-Spengler formation of chiral 1,1’-disubstituted- and spiro-tetrahydroisoquinolines

2. A Titanium(III)-Catalyzed Reductive Umpolung Reaction for the Synthesis of 1,1-Disubstituted Tetrahydroisoquinolines

3. Synthesis of 1,1-Disubstituted Tetrahydroisoquinolines by Lithiation and Substitution, with in Situ IR Spectroscopy and Configurational Stability Studies

4. The Neuroprotective Effect of the Novel Noncompetitive NMDA Antagonist, FR115427 in Focal Cerebral Ischemia in Rats

5. Behavioral studies on FR115427, a novel selective N-methyl-D-aspartate antagonist

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