Zobrazeno 1 - 10
of 629
pro vyhledávání: '"L. Zografos"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 19, Iss 1, Pp 1-26 (2023)
A mature science, combining the art of the total synthesis of complex natural structures and the practicality of delivering highly diverged lead compounds for biological screening, is the constant aim of the organic chemistry community. Delivering na
Externí odkaz:
https://doaj.org/article/6eb8b5d282d743b8800d7c1f45e8514d
Publikováno v:
Organic Chemistry Frontiers. 10:2095-2114
Juggling between reactivity and selectivity, free radical oxidation offers a unique means to synthesize natural products in a direct and efficient way. The case study of sesquiterpenes is illustrative of how modern total synthesis should be conducted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f0aee822ae54ee738c95996cb22db01
https://doi.org/10.1039/d3qo00314k
https://doi.org/10.1039/d3qo00314k
Publikováno v:
Organic Letters. 24:8476-8480
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ce3300a68517d6c81fb358ab69a3ea4
https://doi.org/10.1021/acs.orglett.2c03215
https://doi.org/10.1021/acs.orglett.2c03215
Publikováno v:
Advanced Synthesis & Catalysis. 364:3059-3065
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcea6bce30e6d888b283ffd651380d30
https://doi.org/10.1002/adsc.202200575
https://doi.org/10.1002/adsc.202200575
Publikováno v:
Clinical Nutrition ESPEN. 54:601-602
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0777eb47acb2cc04dfacac6bb2a3492
https://doi.org/10.1016/j.clnesp.2022.09.422
https://doi.org/10.1016/j.clnesp.2022.09.422
Autor:
Nicolaos S. Iordanidis, Alexandros L. Zografos, Christos I. Stathakis, John K. Gallos, Theocharis V. Koftis
Publikováno v:
European Journal of Organic Chemistry. 2021:5058-5062
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36707d778973084cac16b5c5325be1c9
https://doi.org/10.1002/ejoc.202100912
https://doi.org/10.1002/ejoc.202100912
Publikováno v:
Green Chemistry. 23:9172-9178
Pyrrole-proline diketopiperazine (DKP) acts as an efficient mediator for the reduction of dioxygen by Hantzsch ester under mild conditions to allow the aerobic metal-free epoxidation of electron-rich alkenes. Mechanistic crossovers are underlined, ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1c549e4d3390a293149029f27d352b0
https://doi.org/10.1039/d1gc03029a
https://doi.org/10.1039/d1gc03029a
Autor:
Alexandros L. Zografos, Marina Petsi
Publikováno v:
ACS Catalysis. 10:7093-7099
The ability of natural and non-natural dipeptides to act as activators of dioxygen in the absence of metallic co-catalysts is reported here. Proline derived 2,5-diketopiperazines were found active ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7277123c057268d779ec45d786f288bf
https://doi.org/10.1021/acscatal.0c01847
https://doi.org/10.1021/acscatal.0c01847
Publikováno v:
Organicbiomolecular chemistry. 19(40)
The development of a divergent scaffold able to access an array of diverse natural sesquiterpenoids is described. The route unifies the scope of previously reported plans of our group to allow the scalable synthesis of 8,12-furo and lactone sesquiter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf054baa099efa7e4e85e12c724539a6
https://pubmed.ncbi.nlm.nih.gov/34553736
https://pubmed.ncbi.nlm.nih.gov/34553736
Publikováno v:
Organic & Biomolecular Chemistry. 17:5112-5120
We have recently described the synthesis of strained carbocyclic sesquiterpenoid motifs through a highly regioselective cycloisomerization of common enyne acetates, in the presence of platinum(ii) and gold(i) chlorides as catalysts. In this work, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed422e27d858ede950b5459eef1ac793
https://doi.org/10.1039/c9ob00890j
https://doi.org/10.1039/c9ob00890j