Zobrazeno 1 - 10
of 116
pro vyhledávání: '"Guido, Verniest"'
Autor:
Xavier Deraet, Tatiana Woller, Ruben Van Lommel, Prof. Frank De Proft, Prof. Guido Verniest, Prof. Mercedes Alonso
Publikováno v:
ChemistryOpen, Vol 8, Iss 6, Pp 788-806 (2019)
Abstract The performance of density functionals and wavefunction methods for describing the thermodynamics and kinetics of hydride reductions of 2‐substituted cyclohexanones has been evaluated for the first time. A variety of exchange correlation f
Externí odkaz:
https://doaj.org/article/daab18043050465b9d999f373b1c5d60
Autor:
Yennys Hernández-Molina, Guido Verniest, Magaly Casals-Hung, Jorge Acevedo-MartÃnez, Paul Cos
Publikováno v:
ARKIVOC, Vol 2019, Iss 5, Pp 152-162 (2019)
Externí odkaz:
https://doaj.org/article/5ea9aeb5466e492ea2a0df19cbd0949e
Autor:
Jan Willem Thuring, Hanchu Kong, Guido Verniest, Wenbin Wang, Kristof Van Hecke, Lieven Meerpoel, Yongbin Zhao, Vineet Pande, Marta Brambilla, Jonas Verhoeven
Publikováno v:
Synlett. 32:892-896
The stereoselective preparation of a novel 4′-spirocyclopropyl nucleoside analogue has been developed by using a semibenzilic Favorskii rearrangement of a 4′-(2-chloro-3-oxocyclobutyl)spirofuranose as a key step. These chiral spirocyclic intermed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3279e95162d84baaee38defe91b1c22
https://doi.org/10.1055/a-1386-7194
https://doi.org/10.1055/a-1386-7194
Autor:
Zeina Neouchy, Jan Hullaert, Jonas Verhoeven, Lieven Meerpoel, Jan-Willem Thuring, Guido Verniest, Johan Winne
The synthesis of cyclopropyl pinacol boronic esters from dibromocyclopropanes via Matteson–Pasto rearrangement is reported. The method is readily scalable and shows limited levels of stereoinduction, with a selectivity that is in part complementary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cdc3adf115e0176c7967ec1d75f8435
https://biblio.vub.ac.be/vubir/synthesis-of-cyclopropyl-pinacol-boronic-esters-from-dibromocyclopropanes(41234753-b831-4e2e-9931-f543901fa654).html
https://biblio.vub.ac.be/vubir/synthesis-of-cyclopropyl-pinacol-boronic-esters-from-dibromocyclopropanes(41234753-b831-4e2e-9931-f543901fa654).html
Publikováno v:
ARKIVOC, Vol 2012, Iss 5, Pp 6-15 (2011)
Externí odkaz:
https://doaj.org/article/5b04828b8769426cb303078a31f1df99
Autor:
Zeina, Neouchy, Jonas, Verhoeven, Hanchu, Kong, Yongbin, Zhao, Wenbin, Wang, Marta, Brambilla, Kristof, Van Hecke, Lieven, Meerpoel, Jan Willem, Thuring, Guido, Verniest, Johan, Winne
Publikováno v:
The Journal of organic chemistry. 86(23)
Cyclopropane fusion of the only rotatable carbon-carbon bond in furanosyl nucleosides (i.e., exocyclic 4'-5') is a powerful design strategy to arrive at conformationally constrained analogues. Herein, we report a direct stereodivergent route toward t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e5d09aa24eae66e648c46513b08eb948
https://pubmed.ncbi.nlm.nih.gov/34748342
https://pubmed.ncbi.nlm.nih.gov/34748342
Autor:
Guido Verniest, Yongbin Zhao, Lucile Marguerite Jouffroy, Jan Willem Thuring, Hanchu Kong, Jonas Verhoeven, Marta Brambilla, Wenbin Wang, Lieven Meerpoel, Johan M. Winne
Publikováno v:
Organic letters. 23(22)
Novel C-4′,C-5′ cyclobutane-fused spirocyclic ribonucleoside analogues were prepared. Thermal [2 + 2] cycloaddition between dichloroketene and readily derived 4′-exo-methylene furanoses afforded a first entry to the required constrained ribofur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c016ec9e92c62fef46ad8db24971640b
https://pubmed.ncbi.nlm.nih.gov/34978448
https://pubmed.ncbi.nlm.nih.gov/34978448
Autor:
Ann Vos, Freija De Vleeschouwer, Tongfei Wu, Guido Verniest, Jan Willem Thuring, Weimei Sun, Jonas Verhoeven, Hanchu Kong, Vineet Pande, Kristof Van Hecke, Lieven Meerpoel
Publikováno v:
Chemistry – A European Journal. 25:15419-15423
Despite the large variety of modified nucleosides that have been reported, the preparation of constrained 4 '-spirocyclic adenosine analogues has received very little attention. We discovered that the [2+2]-cycloaddition of dichloroketene on readily
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c12a7ae47b86bc5cc43529ad68b53dc9
https://doi.org/10.1002/chem.201904574
https://doi.org/10.1002/chem.201904574
Autor:
Weimei Sun, Jan Willem Thuring, Frank De Proft, Xavier Deraet, Mercedes Alonso, Lieven Meerpoel, Guido Verniest, Jonas Verhoeven, Vineet Pande
Publikováno v:
The Journal of organic chemistry. 85(23)
A novel class of substituted spiro[3.4]octanes can be accessed via a [2 + 2]-cycloaddition of dichloroketene on a readily prepared exo-methylene cyclopentane building block. This reaction sequence was found to be robust on a multigram scale and affor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b94b2bce0899c9cf3b11b13c71587be
https://pubmed.ncbi.nlm.nih.gov/33196210
https://pubmed.ncbi.nlm.nih.gov/33196210
Autor:
Lucile Jouffroy, Jonas Verhoeven, Marta Brambilla, Guido Verniest, Hanchu Kong, Yongbin Zhao, Wenbin Wang, Lieven Meerpoel, Jan Willem Thuring, Johan M. Winne
Publikováno v:
Organic Letters. 24:798-798
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10658d4252f45c231e46f6f9c7676a11
https://doi.org/10.1021/acs.orglett.1c04263
https://doi.org/10.1021/acs.orglett.1c04263