Photocatalyzed Radical Cross-Coupling of Allylic Esters with <i>N</i> -Aryl Glycinates and Benzyl Amines for sp <sup>3</sup> C–C Bond Formation

) bond formation. The approach demonstrates remarkable substrate versatility and functional group compatibility, enabling late-stage derivatization of diverse natural products. The reaction also achieves enantioselective control through chiral auxiliaries, such as (-)-menthol, underscoring its synthetic potential.

Authors

Guoqin Xia (ORCID: https://orcid.org/0000-0001-7666-9550)
Pengli Zhang (ORCID: https://orcid.org/0000-0002-8554-4343)
Xudong Yuan (ORCID: https://orcid.org/0000-0002-8683-4297)
Haihui Huang

Institutions

Guangzhou University of Chinese Medicine (CN)
Nanjing University of Chinese Medicine (CN)
Shanghai Institute of Materia Medica (CN)
Drug Discovery Laboratory (Norway) (NO)
University of Chinese Academy of Sciences (CN)

Publication Details

Journal: Organic Letters
Published: 2026-04-01
DOI: https://doi.org/10.1021/acs.orglett.6c01024
Primary Topic: Radical Photochemical Reactions
Type: article
Field-Weighted Citation Impact: 0.00

Funders

National Natural Science Foundation of China
Zhongshan Science and Technology Bureau

Controls

|||

ALL TIME

JAN

FEB

MAR

APR

MAY

JUN

JUL

AUG

SEP

OCT

article

Photocatalyzed Radical Cross-Coupling of Allylic Esters with N -Aryl Glycinates and Benzyl Amines for sp ³ C–C Bond Formation

Guoqin Xia, Pengli Zhang, Xudong Yuan, Haihui Huang

Apr 1, 2026

Organic Letters

Radical Photochemical Reactions

article

Photocatalyzed Radical Cross-Coupling of Allylic Esters with N -Aryl Glycinates and Benzyl Amines for sp ³ C–C Bond Formation

Guoqin Xia, Pengli Zhang, Xudong Yuan, Haihui Huang

April 1, 2026article en

Abstract

) bond formation. The approach demonstrates remarkable substrate versatility and functional group compatibility, enabling late-stage derivatization of diverse natural products. The reaction also achieves enantioselective control through chiral auxiliaries, such as (-)-menthol, underscoring its synthetic potential.

Organic LettersVol. 28(14)

Guangzhou University of Chinese Medicine (CN), Nanjing University of Chinese Medicine (CN), Shanghai Institute of Materia Medica (CN), Drug Discovery Laboratory (Norway) (NO), University of Chinese Academy of Sciences (CN)

National Natural Science Foundation of China, Zhongshan Science and Technology Bureau

Openalex Percentile: Top 29%

Radical Photochemical Reactions

DOI Source OpenAlex

AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Photocatalyzed Radical Cross-Coupling of Allylic Esters with <i>N</i> -Aryl Glycinates and Benzyl Amines for sp <sup>3</sup> C–C Bond Formation — Guoqin Xia, Pengli Zhang, et al. · Organic Letters (2026) | TGRS Research Map | TGRS