Ni-catalyzed regio- and diastereoselective <i>syn</i> -alkynylamination of unactivated alkenes using alkylamine sources

A nickel-catalyzed selective alkynylamination of unactivated alkenes to access the corresponding homopropargyl amines have been developed. This protocol offers a range of alkylamine sources, including secondary and less sterically hindered primary amines.

Authors

Institutions

Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00194c
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Ni-catalyzed regio- and diastereoselective syn -alkynylamination of unactivated alkenes using alkylamine sources

Yanjian Wan, Cong Lin, Liang Shen, Yang‐Chun Cheng
1 citations
Organic Chemistry Frontiers
Catalytic C–H Functionalization Methods
0.94
article

Ni-catalyzed regio- and diastereoselective syn -alkynylamination of unactivated alkenes using alkylamine sources

Yanjian Wan, Cong Lin, Liang Shen, Yang‐Chun Cheng
article en
1 citations

Abstract

A nickel-catalyzed selective alkynylamination of unactivated alkenes to access the corresponding homopropargyl amines have been developed. This protocol offers a range of alkylamine sources, including secondary and less sterically hindered primary amines.

Organic Chemistry FrontiersVol. 12(14)
Jiangxi Science and Technology Normal University (CN)
Openalex Percentile: Top 28%
Catalytic C–H Functionalization Methods
0.94
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.