Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Dylan J. Twardy"'
Publikováno v:
Molecules, Vol 27, Iss 7, p 2062 (2022)
This review includes recent developments in the synthesis of benzo[4,5]imidazo[2,1-a]isoquinolines with particular attention given to categorizing protocols based on the structural features of the ring architecture and crystallographically characteri
Externí odkaz:
https://doaj.org/article/98089155ad7b48c68f5f7abb7937ae92
Autor:
Mukulesh Mondal, Shi Chen, Manashi Panda, Ahmad A. Ibrahim, Nessan J. Kerrigan, Dylan J. Twardy
Publikováno v:
European Journal of Organic Chemistry. 2020:5752-5764
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::377690ac7d7cb43484100a07eb8d42fc
https://doi.org/10.1002/ejoc.202000976
https://doi.org/10.1002/ejoc.202000976
Autor:
Mukulesh Mondal, Shubhanjan Mitra, Dylan J. Twardy, Manashi Panda, Kraig A. Wheeler, Nessan J. Kerrigan
Publikováno v:
Mondal, Mukulesh, Mitra, Shubhanjan, Twardy, Dylan J., Panda, Manashi, Wheeler, Kraig ORCID: 0000-0001-6752-7542 and Kerrigan, Nessan ORCID: 0000-0003-3643-5260 (2022) Asymmetric synthesis of bicyclic pyrazolidinones through alkaloid-catalyzed [3 + 2]-cycloadditions of ketenes and azomethine imines. Chemistry-A European Journal, 28 (21). ISSN 0947-6539
A versatile asymmetric synthesis of bicyclic pyrazolidinones through alkaloid-catalyzed formal [3 + 2]- and [3 + 2 + 2]-cycloadditions of ketenes with azomethine imines is described. The methodology was found to be tolerant of ketene and a variety of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a50c0c7069785991b786a64ad2ad4e1
http://doras.dcu.ie/28262/
http://doras.dcu.ie/28262/
Autor:
Manisha Mishra, Clifford J. Ellstrom, Béla Török, Roman Dembinski, Dylan J. Twardy, Kraig A. Wheeler
Publikováno v:
Green Chemistry. 21:99-108
An efficient environmentally benign route for the synthesis of benzimidazo[2,1-a]isoquinoline has been developed by reacting 2-ethynylbenzaldehyde and related substituted alkynylbenzaldehydes with variously substituted ortho-phenylenediamines and ali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2553838a23d3d596ec9ad87cddf5ef7
https://doi.org/10.1039/c8gc02520g
https://doi.org/10.1039/c8gc02520g
Autor:
Dariusz Korczyński, Robert Snoeck, Renata Kaczmarek, Dylan J. Twardy, Graciela Andrei, Rafał Dolot, Roman Dembinski, Trevor L. Olson, Kraig A. Wheeler
Publikováno v:
European Journal of Medicinal Chemistry
A novel methodology to access alkynyl nucleoside analogs was elaborated. Highly fluorescent 5-alkynylfuropyrimidines were synthesized (97-46%) and their antiviral properties investigated in vitro. Regiochemistry of the functionalization was achieved
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::931fe762f9f430ea13cd1fe86bf41baf
https://pubmed.ncbi.nlm.nih.gov/33039724
https://pubmed.ncbi.nlm.nih.gov/33039724