Evidence map›Paper›PMID 41512048›Full record

ArticleOrganic letters2026

Bifunctional Monothiosquaramide-Catalyzed Enantioselective Addition of Masked Acyl Cyanide to Isatins: Umpolung Strategy for the Total Synthesis of (

Francisco A A Reis, Manda Sathish, Bárbara V Silva, Roberta K F Marra, Letícia O Magalhães, Viresh H Rawal, Fabiane M Nachtigall, Leonardo S Santos

Abstract read
In one paragraph

Article in Organic letters, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Francisco A A ReisLaboratory of Asymmetric Synthesis, Chemistry Institute of Natural Resources Universidad de Talca Casilla 747, Talca 3460000, Chile.
Manda SathishCentro de Investigación de Estudios Avanzados del Maule, Vicerrectoría de Investigación y Postgrado Universidad Católica del Maule, Avenida San Miguel, Talca 3460000, Chile.
Bárbara V SilvaInstituto de Química, Universidade Federal do Rio de Janeiro, Avenida Athos da Silveira Ramos 149, Cidade Universitaria, Rio de Janeiro, Rio de Janeiro 21949-900, Brazil.
Roberta K F MarraInstituto de Química, Universidade Federal do Rio de Janeiro, Avenida Athos da Silveira Ramos 149, Cidade Universitaria, Rio de Janeiro, Rio de Janeiro 21949-900, Brazil.
Letícia O MagalhãesInstituto de Química, Universidade Federal do Rio de Janeiro, Avenida Athos da Silveira Ramos 149, Cidade Universitaria, Rio de Janeiro, Rio de Janeiro 21949-900, Brazil.
Viresh H RawalDepartment of Chemistry, University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, United States.ORCID 0000-0003-4606-0239
Fabiane M NachtigallInstituto de Ciencias Aplicadas Universidad Autónoma de Chile Talca 3467987, Chile.
Leonardo S SantosLaboratory of Asymmetric Synthesis, Chemistry Institute of Natural Resources Universidad de Talca Casilla 747, Talca 3460000, Chile.ORCID 0000-0002-1697-4200

Funding

New Methods and Strategies for the Concise Synthesis of Complex Indole AlkaloidsR01GM144663 · NIGMS · UNIVERSITY OF CHICAGO · PI RAWAL, VIRESH H. · 2021 to 2024
$1.3M
Methods and Strategies for Concise Syntheses of Intricate Bioactive CompoundsR35GM158168 · NIGMS · UNIVERSITY OF CHICAGO · PI VIRESH H. RAWAL · 2025 to 2026
$850k
NIGMS NIH HHS R01 GM144663NIGMS NIH HHS R35 GM158168
6 · The paper itself

Abstract

The enantioselective addition of masked acyl cyanide (MAC) to isatin is a highly efficient strategy for synthesizing bioactive chiral spirooxindoles. Herein, we report the utility of this strategy in an asymmetric total synthesis of (

Identifiers

PMID41512048
PMCPMC13050229

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.