One-Pot Reaction Sequence: <i>N</i>-Acylation/Pictet–Spengler Reaction/Intramolecular [4 + 2] Cycloaddition/Aromatization in the Synthesis of β-Carboline Alkaloid Analogues-Reference-Cited by-同舟云学术

One-Pot Reaction Sequence: N-Acylation/Pictet–Spengler Reaction/Intramolecular [4 + 2] Cycloaddition/Aromatization in the Synthesis of β-Carboline Alkaloid Analogues

Published:2024-02-15 Issue:5 Volume:89 Page:3065-3071
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Alekseeva Kseniya A.¹,Fedoseeva Milana A.¹,Bakhanovich Olga V.¹²,Khrustalev Victor N.³⁴,Potkin Vladimir I.⁵,Zhou Hongwei⁶^ORCID,Nikitina Eugenia V.¹,Zaytsev Vladimir P.¹^ORCID,Zubkov Fedor I.¹^ORCID

Affiliation:

1. Organic Chemistry Department, Faculty of Science, RUDN University, 6 Miklukho-Maklaya St., Moscow 117198, Russian Federation

2. Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo náměstí 2, Prague 166 10, Czech Republic

3. N. D. Zelinsky Institute of Organic Chemistry of Russian Academy of Sciences, Moscow 119991, Russia

4. Inorganic Chemistry Department, Faculty of Science, RUDN University, 6 Miklukho-Maklaya St., Moscow 117198, Russian Federation

5. Institute of Physical Organic Chemistry of National Academy of Sciences of Belarus, 13 Surganov Street, Minsk 220072, Belarus

6. Jiaxing University, 1 Jiahang Road, Jiaxing, Zhejiang 314001, China

Funder

Russian Science Foundation

Belarusian Republican Foundation for Fundamental Research

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c02533

Reference34 articles.

1. Recent Advances in the Synthesis of β-Carboline Alkaloids

2. A Comprehensive Review on Recent Advances in Synthesis and Pharmacotherapeutic Potential of Betacarbolines

3. Recent Insights into β-Carboline Alkaloids with Anticancer Potential

4. β-Carboline alkaloid monomers and dimers: Occurrence, structural diversity, and biological activities

5. An overview on synthetic entries to tetrahydro-β-carbolines