A novel synthesis of functionalized spirooxaphospholes

The reaction of ethyl propiolate with triphenylphosphine in the presence of N-alkylisatins led to ethyl oxaphosphole in good yields. The reaction of dialkyl acetylenedicarboxylates with Ph3P in the presence of N-alkylisatins led to oxaphosphole-3,4-dicarboxylate in good yields.

Authors

Publication Details

Published
2025-03-24
DOI
https://doi.org/10.82361/iranjoc.2025.1202655
Primary Topic
Phosphorus compounds and reactions
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A novel synthesis of functionalized spirooxaphospholes

IAU
Phosphorus compounds and reactions
article

A novel synthesis of functionalized spirooxaphospholes

IAU
article en

Abstract

The reaction of ethyl propiolate with triphenylphosphine in the presence of N-alkylisatins led to ethyl oxaphosphole in good yields. The reaction of dialkyl acetylenedicarboxylates with Ph3P in the presence of N-alkylisatins led to oxaphosphole-3,4-dicarboxylate in good yields.

Openalex Percentile: Top 32%
Phosphorus compounds and reactions
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.

A novel synthesis of functionalized spirooxaphospholes — IAU · (2025) | TGRS Research Map | TGRS