Evidence map›Paper›PMID 21918584›Full record

ArticleSynthesis2011

Developing novel organocatalyzed aldol reactions for the enantioselective synthesis of biologically active molecules.

Mayur Bhanushali, Cong-Gui Zhao

Abstract read
In one paragraph

Article in Synthesis, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

2 authors.

Mayur BhanushaliDepartment of Chemistry, University of Texas at San Antonio, One UTSA Circle, San Antonio, Texas 78249-0698, USA.
Cong-Gui Zhao

Funding

UTSA MBRS SCORE PROGRAMS06GM008194 · NIGMS · UNIVERSITY OF TEXAS SAN ANTONIO · PI TSIN, ANDREW T C · 1989 to 2006
$17.4M
Enantioselective Synthesis of Phosphinate DerivativesSC1GM082718 · NIGMS · UNIVERSITY OF TEXAS SAN ANTONIO · PI ZHAO, JOHN CONG-GUI · 2009 to 2012
$1.0M
NIGMS NIH HHS S06 GM008194NIGMS NIH HHS SC1 GM082718
6 · The paper itself

Abstract

Aldol reaction is one of the most important methods for the formation of carbon-carbon bonds. Because of its significance and usefulness, asymmetric versions of this reaction have been realized with different approaches in the past. Over the last decade, the area of organocatalysis has made significant progresses. As one of most studied reactions in organocatalyses, organocatalyzed aldol reaction has emerged as a powerful tool for the synthesis of a large number of useful products in optically enriched forms. In this review, we summarize our efforts on the development of novel organocatalyzed aldol reactions for the enantioselective synthesis of biological active molecules. Literatures closely related to our studies are also covered.

Identifiers

PMID21918584
PMCPMC3170696

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.