HFIP-promoted halo-carbocyclizations of <i>N</i>- and <i>O</i>-tethered arene–alkene substrates to access all halo (X = Br, I, Cl)-functionalized tetrahydroquinoline and chroman cores-Reference-Cited by-同舟云学术

HFIP-promoted halo-carbocyclizations of N- and O-tethered arene–alkene substrates to access all halo (X = Br, I, Cl)-functionalized tetrahydroquinoline and chroman cores

Published:2022 Issue:41 Volume:20 Page:8136-8144
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Shukla Pushpendra Mani¹,Bhattacharya Aditya¹,Pratap Aniruddh¹,Pradhan Akash¹,Sinha Puspita¹,Soni Tanishk¹^ORCID,Maji Biswajit¹^ORCID

Affiliation:

1. Department of Chemistry, Indira Gandhi National Tribal University, Amarkantak-484886, Madhya Pradesh, India

Abstract

Herein, a HFIP-promoted mild and efficient method for the synthesis of all halo (X = Br, I, Cl)-functionalized tetrahydroquinoline and chroman building blocks is disclosed.

Funder

Science and Engineering Research Board

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB01597H

Reference101 articles.

1. HFIP in Organic Synthesis

2. Cover Picture: Continuous‐Flow Suzuki‐Miyaura and Mizoroki‐Heck Reactions under Microwave Heating Conditions (Chem. Rec. 1/2019)

3. Hexafluoroisopropanol as a highly versatile solvent