A radical 1,4-aryl migration enables nickel-catalysed remote cross-electrophile coupling of β-bromo amino acid esters with vinyl triflates

A radical 1,4-aryl migration enabling a cross-electrophile coupling reaction toward remote transalkylation of N-benzyl alanine has been developed. In this strategy, with the occurrence of a radical-mediated Turce-Smiles rearrangement, key α-aminoalkyl radicals are generated. The as-formed α-aminoalkyl radical serves as a robust coupling partner for cross-electrophilic coupling with vinyl triflates, affording a series of olefin-tethered amino acid motifs.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:60

Enthalten in:

Chemical communications (Cambridge, England) - 60(2024), 32 vom: 16. Apr., Seite 4306-4309

Sprache:

Englisch

Beteiligte Personen:

Liu, Yin-Ling [VerfasserIn]
Liu, Jian [VerfasserIn]
Li, Xin-Yu [VerfasserIn]
He, Peng [VerfasserIn]
Liu, Yu-Xuan [VerfasserIn]
Xiang, Mei [VerfasserIn]
Tang, Shi [VerfasserIn]

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Date Revised 16.04.2024

published: Electronic

Citation Status PubMed-not-MEDLINE

doi:

10.1039/d4cc00627e

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM370231090