Evidence map›Paper›PMID 36014353›Full record

ArticleMolecules (Basel, Switzerland)2022

Synthesis and Stereochemical Characterization of a Novel Chiral α-Tetrazole Binaphthylazepine Organocatalyst.

Assunta Summa, Patrizia Scafato, Sandra Belviso, Guglielmo Monaco, Riccardo Zanasi, Giovanna Longhi, Sergio Abbate, Stefano Superchi

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 44% of its field
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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 3 institutions in 1 country.

Assunta SummaDepartment of Sciences, University of Basilicata, Via dell'Ateneo Lucano 10, 85100 Potenza, Italy.
Patrizia ScafatoDepartment of Sciences, University of Basilicata, Via dell'Ateneo Lucano 10, 85100 Potenza, Italy.
Sandra BelvisoDepartment of Sciences, University of Basilicata, Via dell'Ateneo Lucano 10, 85100 Potenza, Italy.ORCID 0000-0002-2997-0129
Guglielmo MonacoDepartment of Chemistry and Biology "A. Zambelli", University of Salerno, Via Giovanni Paolo II, 84084 Salerno, Italy.ORCID 0000-0001-5268-940X
Riccardo ZanasiDepartment of Chemistry and Biology "A. Zambelli", University of Salerno, Via Giovanni Paolo II, 84084 Salerno, Italy.ORCID 0000-0002-8374-6080
Giovanna LonghiDepartment Molecular and Translational Medicine, University of Brescia, viale Europa 11, 25123 Brescia, Italy.ORCID 0000-0002-0011-5946
Sergio AbbateDepartment Molecular and Translational Medicine, University of Brescia, viale Europa 11, 25123 Brescia, Italy.ORCID 0000-0001-9359-1214
Stefano SuperchiDepartment of Sciences, University of Basilicata, Via dell'Ateneo Lucano 10, 85100 Potenza, Italy.ORCID 0000-0002-7265-1625
University of Basilicata · ITUniversity of Brescia · ITUniversity of Salerno · IT

Funding

Ministry of Education, Universities and Research ARS01_00985
6 · The paper itself

Abstract

A novel α-tetrazole-substituted 1,1'-binaphthylazepine chiral catalyst has been synthesized and its absolute configuration has been determined by DFT computational analysis of the vibrational circular dichroism (VCD) spectrum of its precursor. The VCD analysis, carried out through the model averaging method, allowed to assign the absolute configuration of a benzylic stereocenter in the presence of a chiral binaphthyl moiety. The 1,1'-binaphthylazepine tetrazole and the nitrile its immediate synthetic precursor, have been preliminarily tested as chiral organocatalysts in the asymmetric intramolecular oxa-Michael cyclization of 2-hydroxy chalcones for the synthesis of chiral flavanones obtaining low enantioselectivity.

Indexed as

TetrazolesCircular DichroismMolecular ConformationStereoisomerismTetrazolesabsolute configurationbinaphthylazepinesflavanonesorganocatalysisvibrational circular dichroism

Identifiers

PMID36014353
PMCPMC9413694
OpenAlexW4290998901

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.