Evidence map›Paper›PMID 41376189›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Enantioselective Syntheses of Secondary Alkylboronates via Asymmetric Regioselective Reduction of 1,3-Dienylboronates.

Wen-Bin Cao, Lingfei Hu, Jiaming Liu, George Chen, Gang Lu, Ming Chen

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Asymmetric Ketone Diene Coupling via Stereodivergent Copper Catalysis.Journal of the American Chemical Society · 2026
    Article
  3. Article
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

6 authors.

Wen-Bin Cao *Department of Chemistry, Virginia Tech, Blacksburg, VA, 24061, United States.
Lingfei Hu *School of Chemistry and Chemical Engineering, Shandong University, Jinan, Shandong, 250100, P. R. China.
Jiaming LiuSchool of Chemistry & Materials, Jiangsu Provincial Key Laboratory of Green & Functional Materials and Environmental Chemistry, Yangzhou University, Yangzhou, Jiangsu, 225000, China.
George ChenDepartment of Chemistry, Virginia Tech, Blacksburg, VA, 24061, United States.
Gang LuSchool of Chemistry and Chemical Engineering, Shandong University, Jinan, Shandong, 250100, P. R. China.
Ming ChenDepartment of Chemistry, Virginia Tech, Blacksburg, VA, 24061, United States.ORCID https://orcid.org/0000-0002-9841-8274

Funding

Asymmetric Synthesis via Organoboron CompoundsR35GM147523 · NIGMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI Ming Chen · 2022 to 2026
$1.9M
National Natural Science Foundation of China 21973055National Natural Science Foundation of China 22371171NIGMS NIH HHS R35 GM147523NIH HHS R35 GM147523-01Postdoctoral Fellowship Program of CPSF GZC20231441
6 · The paper itself

Abstract

We report herein the development of catalytic asymmetric synthesis of secondary alkylboronates. Under the optimal conditions, Cu-catalyzed semi-reduction of 1-alkyl- or 1,3-dialkyl-substituted 1-boryl-1,3-butadienes forms secondary alkylboronates with excellent regioselectivities and enantioselectivities. With H

Indexed as

Asymmetric synthesesCopper catalysisDiene semi‐reductionRegioselectiveSecondary alkylboronates

Identifiers

PMID41376189
PMCPMC12811667

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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 Socratic graph.