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

Morla, Jhansi Rani; Nareddula, Dastagiri Reddy

doi:10.1039/d2ra00389a

RSC Adv.

2022

DOI: 10.1039/d2ra00389a

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

Jhansi Rani Morla

Dastagiri Reddy Nareddula

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].

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2024

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Palladium-catalyzed cyclization borylmethylation: Access to boryl-functionalized benzene-fused heterocycle compounds

Li,

Ye,

Cui

et al. 2024

Tetrahedron Letters

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Palladium-catalyzed cyclization borylmethylation: Access to boryl-functionalized benzene-fused heterocycle compounds

Li,

Ye,

Cui

et al. 2024

Tetrahedron Letters

View full text Add to dashboard Cite

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

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].

Cited by 1 publication

References 49 publications

Palladium-catalyzed cyclization borylmethylation: Access to boryl-functionalized benzene-fused heterocycle compounds

Palladium-catalyzed cyclization borylmethylation: Access to boryl-functionalized benzene-fused heterocycle compounds

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