I<sub>2</sub>‑Promoted\nChemoselective Annulative\nCoupling of 2‑Aminobenzamides with Sulfoxonium Ylides: Easy\nAccess to Quinazolinones

A flexible and metal-free synthetic approach for synthesizing\n2-benzoyl\nquinazolinones and 2-aryl quinazolinones via molecular iodine-mediated\nannulative coupling of sulfoxonium ylides with 2-aminobenzamides has\nbeen disclosed. The method demonstrates remarkable chemoselectivity\nand efficiency, leading to high yields of 2-benzoyl quinazolinones\nand 2-aryl quinazolinones under optimized conditions. The broad substrate\nscope, scalability, and practical utility were highlighted through\ndiverse applications, including gram-scale reactions and the synthesis\nof biologically significant compounds such as tryptanthrin and the\nchemo/biosensor derivative.

Publication Details

Journal
Figshare
Published
2024-08-20
DOI
https://doi.org/10.1021/acs.joc.4c01354.s001
Primary Topic
Quinazolinone synthesis and applications
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

I2‑Promoted\nChemoselective Annulative\nCoupling of 2‑Aminobenzamides with Sulfoxonium Ylides: Easy\nAccess to Quinazolinones

Figshare
Quinazolinone synthesis and applications
article

I2‑Promoted\nChemoselective Annulative\nCoupling of 2‑Aminobenzamides with Sulfoxonium Ylides: Easy\nAccess to Quinazolinones

article en

Abstract

A flexible and metal-free synthetic approach for synthesizing\n2-benzoyl\nquinazolinones and 2-aryl quinazolinones via molecular iodine-mediated\nannulative coupling of sulfoxonium ylides with 2-aminobenzamides has\nbeen disclosed. The method demonstrates remarkable chemoselectivity\nand efficiency, leading to high yields of 2-benzoyl quinazolinones\nand 2-aryl quinazolinones under optimized conditions. The broad substrate\nscope, scalability, and practical utility were highlighted through\ndiverse applications, including gram-scale reactions and the synthesis\nof biologically significant compounds such as tryptanthrin and the\nchemo/biosensor derivative.

Figshare
Openalex Percentile: Top 76%
Quinazolinone synthesis and applications
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.

I<sub>2</sub>‑Promoted\nChemoselective Annulative\nCoupling of 2‑Aminobenzamides with Sulfoxonium Ylides: Easy\nAccess to Quinazolinones · Figshare (2024) | TGRS Research Map | TGRS