Three-Component, Diastereoselective Prins–Ritter Reaction for cis-Fused 4-Amidotetrahydropyrans toward a Precursor for Possible Neuronal Receptor Ligands-Reference-Cited by-同舟云学术

Three-Component, Diastereoselective Prins–Ritter Reaction for cis-Fused 4-Amidotetrahydropyrans toward a Precursor for Possible Neuronal Receptor Ligands

Published:2016-05-17 Issue:7 Volume:18 Page:399-404
ISSN:2156-8952
Container-title:ACS Combinatorial Science
language:en
Short-container-title:ACS Comb. Sci.

Author:

Chiba Manami¹,Ishikawa Yuichi¹,Sakai Ryuichi¹,Oikawa Masato¹

Affiliation:

1. Yokohama City University, Seto 22-2, Kanazawa-ku, Yokohama 236−0027, Japan

Funder

Ministry of Education, Culture, Sports, Science, and Technology

Publisher

American Chemical Society (ACS)

Subject

General Chemistry,General Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/acscombsci.6b00046

Reference36 articles.

1. Synthesis of tetrahydropyrans and related heterocycles via prins cyclization; extension to aza-prins cyclization

2. Synthesis of (−)-Centrolobine by Prins Cyclizations that Avoid Racemization

3. Stereoselective Synthesis of the Tetrahydropyran Core of Polycarvernoside A

4. Prins Cyclizations in Silyl Additives with Suppression of Epimerization: Versatile Tool in the Synthesis of the Tetrahydropyran Backbone of Natural Products

Cited by 29 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ritter-Type Reaction;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2024

2. A Brief Review on Proved Approaches for the Formation of Oxygen Containing Heterocyclic Compounds through a Tandem Prins Cyclization;Mini-Reviews in Organic Chemistry;2023-09

3. Total synthesis of lycoperdic acid and stereoisomers (part 2): Completion of the synthesis and biological evaluation;Tetrahedron;2023-09

4. Acid Catalyzed Multicomponent Reaction to Access Functionalized N‐Benzhydryl Amides: A Tandem Ritter Reaction;European Journal of Organic Chemistry;2023-07-27

5. Sugars in Multicomponent Reactions: A Toolbox for Diversity-Oriented Synthesis;Synthesis;2023-03-02