Gelson Perin

Prof. Gelson Perin

orcid

Research Focus & Metrics

Academic Career Length

32Years (1995-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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17 February 2009 in Chemical Reviews
Verified
Journal Article
Closed access
GPGelson Perin
Gelson Perin
Eder LenardaoEder Lenardao
Eder Lenardao
RJRaquel Jacob
Raquel Jacob
RPRodrigo Barroso Panatieri
Rodrigo Barroso Panatieri

16 April 2019 in Chemical Reviews
Verified
Journal Article
Closed access
Filipe PenteadoFilipe Penteado
Filipe Penteado
ELEric Lopes
Eric Lopes
Diego AlvesDiego Alves
Diego Alves
GPGelson Perin
Gelson Perin
RJRaquel Jacob
Raquel Jacob
Eder LenardaoEder Lenardao
Eder Lenardao

1 July 2007 in Tetrahedron
Verified
Journal Article
Closed access
Eder LenardaoEder Lenardao
Eder Lenardao
GBGiancarlo V. Botteselle
Giancarlo V. Botteselle
Francisco de AzambujaFrancisco de Azambuja
Francisco de Azambuja
GPGelson Perin
Gelson Perin
RJRaquel Jacob
Raquel Jacob

1 August 2012 in Food and Chemical Toxicology
Verified
Journal Article
Closed access
FVFrancine Novack Victoria
Francine Novack Victoria
Eder LenardaoEder Lenardao
Eder Lenardao
LSLucielli Savegnago
Lucielli Savegnago
GPGelson Perin
Gelson Perin
RJRaquel Jacob
Raquel Jacob
PNPatricia da Silva Nascente
Patricia da Silva Nascente

24 February 2012 in Green Chemistry
Verified
Journal Article
Closed access
PDF file
VRVanessa G. Ricordi
Vanessa G. Ricordi
CFCamilo S. Freitas
Camilo S. Freitas
GPGelson Perin
Gelson Perin
Eder LenardaoEder Lenardao
Eder Lenardao
RJRaquel Jacob
Raquel Jacob
Diego AlvesDiego Alves
Diego Alves
We describe herein the use of glycerol as the solvent in the copper-catalyzed cross-coupling reaction of diaryl diselenides with arylboronic acids using CuI and DMSO as additive. This cross-coupling reaction was performed with diaryl diselenides and arylboronic acids bearing electron-withdrawing and electron-donating groups, affording the corresponding diaryl selenides in good to excellent yields. The glycerol–CuI mixture can be directly reused for further cross-coupling reactions.

29 May 2021 in Applied Sciences
Verified
Journal Article
Open access
PDF file
Patrick RollinPatrick Rollin
Patrick Rollin
LSLiane K. Soares
Liane K. Soares
Angelita Manke BarcellosAngelita Manke Barcellos
Angelita Manke Barcellos
DADaniela Rodrigues Araujo
Daniela Rodrigues Araujo
Eder LenardaoEder Lenardao
Eder Lenardao
GPGelson Perin
Gelson Perin
This review presents the recent advances involving several applications of five-membered cyclic carbonates and derivatives. With more than 150 references, it covers the period from 2012 to 2020, with special emphasis on the use of five-membered cyclic carbonates as building blocks for organic synthesis and material elaboration. We demonstrate the application of cyclic carbonates in several important chemical transformations, such as decarboxylation, hydrogenation, and transesterification reactions, among others. The presence of cyclic carbonates in molecules with high biological potential is also displayed, together with the importance of these compounds in the preparation of materials such as urethanes, polyurethanes, and flame retardants.