Hypervalent Iodine‐Mediated and Traceless Fluorine‐Oriented: Synthesis of 5‐Methyl‐1,2,3,4‐tetrahydropyridine from Unactivated Alkenes-Reference-Cited by-同舟云学术

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Hypervalent Iodine‐Mediated and Traceless Fluorine‐Oriented: Synthesis of 5‐Methyl‐1,2,3,4‐tetrahydropyridine from Unactivated Alkenes

Published:2021-06-29 Issue:8 Volume:10 Page:2147-2151
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J. Org. Chem.

Author:

Zhang Lu‐Wen¹,Huang Xie²,Wang Jia‐Qi¹,He Wei¹^ORCID

Affiliation:

1. Department of Chemistry School of Pharmacy The Fourth Military Medical University Xi'an 710032 P. R. China

2. State Key Laboratory of Trauma Burns and Combined Injury Institute of Combined Injury Chongqing Engineering Research Center for Nanomedicine Department College of Preventive Medicine Third Military Medical University Chongqing 400038 P. R. China

Publisher

Wiley

Subject

Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajoc.202100290

Reference86 articles.

2. Detailed Investigation of the Production of the Bread Flavor Component 6-Acetyl-1,2,3,4-tetrahydropyridine in Proline/1,3-Dihydroxyacetone Model Systems

3. A novel one-pot four-component access to tetrahydro-β-carbolines by a coupling-amination-aza-annulation-Pictet–Spengler sequence (CAAPS)

4. An Expeditious, High-Yielding Construction of the Food Aroma Compounds 6-Acetyl-1,2,3,4-tetrahydropyridine and 2-Acetyl-1-pyrroline

5. 3,4-trans-4-Aryl-3-(1-pyridinio)-1,2,3,4-tetrahydropyridine-6-thiolates—new group of potential cardiotonic drugs

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