A facile approach for the synthesis of novel 1-oxa- and 1-aza-flavonyl-4-methyl-1H-benzo[d][1,3]oxazin-2(4H)-ones by microwave enhanced Suzuki–Miyaura coupling using bidentate chromen-4-one-based Pd(ii)–diimine complex as catalyst-Reference-Cited by-同舟云学术

A facile approach for the synthesis of novel 1-oxa- and 1-aza-flavonyl-4-methyl-1H-benzo[d][1,3]oxazin-2(4H)-ones by microwave enhanced Suzuki–Miyaura coupling using bidentate chromen-4-one-based Pd(ii)–diimine complex as catalyst

Published:2015 Issue:94 Volume:5 Page:77075-77087
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Kumar Sumit¹²³⁴,Ahmed Naseem¹²³⁴

Affiliation:

1. Department of Chemistry

2. Indian Institute of Technology Roorkee

3. Roorkee 247 667

4. India

Abstract

A facile access to novel 1-oxa- and 1-aza-flavonyl-4-methyl-1H-benzo[d][1,3]oxazin-2(4H)-ones using microwave assisted Suzuki coupling of bromo flavones with boronic acids using a novel catalytic system (C) under aerobic condition is reported.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA15274G

Reference69 articles.

1. Palladium-catalyzed cross-coupling reaction of organoboron compounds with organic triflates

2. Palladium-Catalyzed Cross-Coupling Reactions in Total Synthesis

3. Total Synthesis of (+)-Neopeltolide

4. Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands

5. Highly Efficient Monophosphine-Based Catalyst for the Palladium-Catalyzed Suzuki−Miyaura Reaction of Heteroaryl Halides and Heteroaryl Boronic Acids and Esters

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