Highly stereoselective synthesis of <i>N</i> -sulfonyl amidines with calcium carbide as an acetylene source

A practical and convenient approach for the highly stereoselective synthesis of N -sulfonyl amidines via a one-pot multi-component cascade reaction of sulfonyl azides, amines, water, and calcium carbide as an acetylene source has been developed.

Authors

Institutions

Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo01010a
Citations
3
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
1.61
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Highly stereoselective synthesis of N -sulfonyl amidines with calcium carbide as an acetylene source

Wenfeng Cui, Peiming Gu, Meng‐Xue Wei, Rui An
3 citations
Organic Chemistry Frontiers
Asymmetric Hydrogenation and Catalysis
1.61
article

Highly stereoselective synthesis of N -sulfonyl amidines with calcium carbide as an acetylene source

Wenfeng Cui, Peiming Gu, Meng‐Xue Wei, Rui An
article en
3 citations

Abstract

A practical and convenient approach for the highly stereoselective synthesis of N -sulfonyl amidines via a one-pot multi-component cascade reaction of sulfonyl azides, amines, water, and calcium carbide as an acetylene source has been developed.

Organic Chemistry FrontiersVol. 12(23)
Ningxia University (CN)
Openalex Percentile: Top 15%
Asymmetric Hydrogenation and Catalysis
1.61
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.