Synthesis of dihydroisoquinolinone-4-methylboronic esters <i>via</i> domino Heck/borylation using a structurally characterized palladacycle as a catalyst-Reference-Cited by-同舟云学术

Synthesis of dihydroisoquinolinone-4-methylboronic esters via domino Heck/borylation using a structurally characterized palladacycle as a catalyst

Published:2022 Issue:11 Volume:12 Page:6762-6771
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Morla Jhansi Rani¹,Nareddula Dastagiri Reddy¹^ORCID

Affiliation:

1. Department of Chemistry, Pondicherry University, Pondicherry 605014, India

Abstract

Synthesis of dihydroisoquinolinone-4-methylboronic esters from N-allylcarboxamides and B2(Pin)2via domino Heck/borylation has been achieved by using a quinoxaline-based NHC-palladacycle [Pd(C∧C:)PPh3Cl].

Funder

Department of Science and Technology, Ministry of Science and Technology, India

Council of Scientific and Industrial Research, India

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/RA/D2RA00389A

Reference47 articles.

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2. Synthesis of novel isoquinolinone and 1,2-dihydroisoquinoline scaffolds via Ugi reaction and ring opening reaction of furans

3. Rapid and Atom Economic Synthesis of Isoquinolines and Isoquinolinones by C-H/N-N Activation Using a Homogeneous Recyclable Ruthenium Catalyst in PEG Media

4. Palladium-Catalyzed α-Arylation of Silylenol Ethers in the Synthesis of Isoquinolines and Phenanthridines

5. α-Arylation of Silyl Enol Ethers via Rhodium(III)-Catalyzed C–H Functionalization

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