Evidence map›Paper›PMID 42801533›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Integrating Kinetics into Synthetic Studies via Adaptable Concentration-Dependent Yield Analysis.

Xinyi Xiao, Koki Ikemoto, Toshiya M Fukunaga, Hideaki Nishina, Hiroyuki Isobe

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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.

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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

5 authors.

Xinyi Xiao *Department of Chemistry, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0003-3475-7194
Koki Ikemoto *Department of Chemistry, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0003-4186-7156
Toshiya M Fukunaga *Department of Chemistry, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0001-6402-2346
Hideaki NishinaDepartment of Chemistry, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.ORCID https://orcid.org/0009-0004-2028-7624
Hiroyuki IsobeDepartment of Chemistry, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0001-8907-0694

Funding

JSPS KAKENHI 25H00003JSPS KAKENHI 26K01485JSPS KAKENHI 26K17832JST ACT-X JPMJAX23DIJST PRESTO JPMJPR24M1JST SPRING JPMJSP2108
6 · The paper itself

Abstract

When inversion of optical rotation was discovered during the hydrolysis of sucrose, the name "invert sugar" was coined for this sweetener. The inversion process sparked the field of chemical kinetics by introducing time-course analyses and differential rate equations as important tools for studying reaction mechanisms and rates. These tools have become indispensable in kinetic studies and have also advanced other fields, including biochemistry and the chemical industry. In this study, chemical kinetics are integrated into synthetic studies. The modeling approaches in this study, i.e., machine-learning (ML) modeling of yield distributions and Euler-integration-based modeling of kinetics, are found to be sufficiently versatile and adaptable to accommodate chemical and operational considerations, allowing concentration-dependent yield analysis (CYAN) to reveal kinetics hidden behind synthetic yield data. Importantly, the ML+CYAN approach reveals unexpected aspects of metal-templated oligomeric macrocyclization, particularly the retardation of oligomer-oligomer coupling. The versatility of the approach is further demonstrated through kinetic analysis of existing yield datasets reported in Wilhelmy's classic 1850 paper on chemical kinetics. This approach is practical enough to be integrated into synthetic studies as an add-on module that provides mechanistic and kinetic insights.

Indexed as

concentration‐dependent yield analysiskineticsmacrocyclesorganic synthesistemplate synthesis

Identifiers

PMID42801533
PMCPMC13616260

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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.