Metal-free annulation of β-acylamino ketones: facile access to spirooxazolines and oxazolines via oxidative C–O bond formation-Reference-Cited by-同舟云学术

Metal-free annulation of β-acylamino ketones: facile access to spirooxazolines and oxazolines via oxidative C–O bond formation

Published:2018 Issue:4 Volume:5 Page:544-548
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Chavan Santosh S.¹²³⁴,Rupanawar Bapurao D.¹²³⁴,Kamble Rohit B.¹²³⁴,Shelke Anil M.¹²³⁴,Suryavanshi Gurunath¹²³⁴^ORCID

Affiliation:

1. Chemical Engineering & Process Development Division

2. CSIR-National Chemical Laboratory

3. Pune-411008

4. India

Abstract

A metal-free annulation reaction of β-acylamino ketone derivatives has been reported for the synthesis of a group of functionalized spirooxazolines and oxazolines in good to excellent yields.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/QO/C7QO00783C

Reference59 articles.

1. Enantioselective gem-Chlorofluorination of Active Methylene Compounds Using a Chiral Spiro Oxazoline Ligand

2. Highly Enantioselective Chlorination of β-Keto Esters and Subsequent SN2 Displacement of Tertiary Chlorides: A Flexible Method for the Construction of Quaternary Stereogenic Centers

3. Catalytic Stereoselective Synthesis of Diverse Oxindoles and Spirooxindoles from Isatins

4. Antibacterial Agents That Inhibit Lipid A Biosynthesis

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