Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Myron Triantafyllakis"'
Autor:
Myron Triantafyllakis
Στην εργασία αυτή παρουσιάζονται 5 νέες συνθετικές μεθοδολογίες που εκκινούνται από την οξείδωση απλών φουρανίων. Σαν οξειδωτικό χρησι
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d390df2dbd955b0578f2612189aca15
https://doi.org/10.12681/eadd/43746
https://doi.org/10.12681/eadd/43746
Autor:
Myron Triantafyllakis, Kalliopi Sfakianaki, Dimitris Kalaitzakis, Georgios Vassilikogiannakis
Publikováno v:
Organic Letters. 20:3631-3634
A straightforward synthesis of substituted 2-oxindoles, 3-hydroxy-2-oxindoles, and isatins has been developed. Easily accessible furans were transformed into tetrahydropyranopyrrolones by a singlet oxygen initiated cascade reaction sequence. An acid-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cd7b6cbc6af4ea33957dbe80630e64c
https://doi.org/10.1021/acs.orglett.8b01404
https://doi.org/10.1021/acs.orglett.8b01404
Autor:
Manolis Sofiadis, Myron Triantafyllakis, Konstantinos Daskalakis, Georgios Vassilikogiannakis, Dimitris Kalaitzakis
Publikováno v:
Organic Letters
Asymmetric and site-selective formal [3 + 2]-annulations of γ-alkyl-β,γ-unsaturated γ-lactams with α,β-unsaturated aldehydes have been developed. These organocatalysed transformations yield high value enantioenriched bicyclic γ-lactams with up
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52c4d95235318867bcfa736fdff89ef4
https://pubmed.ncbi.nlm.nih.gov/29417818
https://pubmed.ncbi.nlm.nih.gov/29417818
Autor:
Georgios Vassilikogiannakis, Georgios I. Ioannou, Myron Triantafyllakis, Dimitris Kalaitzakis
A highly efficient and general singlet-oxygen-initiated one-pot transformation of readily accessible furans into octahydroindole scaffolds has been developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b7c4b7a0a234504fb58819916701cd4
https://zenodo.org/record/853052
https://zenodo.org/record/853052
Autor:
Georgios Vassilikogiannakis, Dimitris Kalaitzakis, Myron Triantafyllakis, Manolis Stratakis, Tamsyn Montagnon
Publikováno v:
Chem. Commun.. 50:15480-15498
The purpose of this article is to give a taste of just how powerful the union between furans and photochemically-generated singlet oxygen is proving to be as a synthetic tool and to suggest that this chemistry is only now really coming of age. In att
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc4c999fc5cbff0f1374901f26488317
https://doi.org/10.1039/c4cc02083a
https://doi.org/10.1039/c4cc02083a
Autor:
Manolis Sofiadis, Dimitris Noutsias, Myron Triantafyllakis, Dimitris Kalaitzakis, Georgios Vassilikogiannakis
Publikováno v:
ChemInform. 47
A highly adaptable method targeting the ubiquitous and very important pyrrolizidine and indolizidine scaffolds is presented. The general synthetic utility of the method is underscored by its application to the rapid and easy synthesis of five natural
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3d78b23f2fbf8b7e99808e0b84b2f9b
https://doi.org/10.1002/chin.201631040
https://doi.org/10.1002/chin.201631040
Autor:
Manolis Sofiadis, Dimitris Noutsias, Georgios Vassilikogiannakis, Myron Triantafyllakis, Dimitris Kalaitzakis
Publikováno v:
Angewandte Chemie (International ed. in English). 55(14)
A highly adaptable method targeting the ubiquitous and very important pyrrolizidine and indolizidine scaffolds is presented. The general synthetic utility of the method is underscored by its application to the rapid and easy synthesis of five natural
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2dad0a74836c98911954108367ad411
https://pubmed.ncbi.nlm.nih.gov/26934056
https://pubmed.ncbi.nlm.nih.gov/26934056
Autor:
Manolis Sofiadis, Georgios Vassilikogiannakis, Myron Triantafyllakis, Dimitris Kalaitzakis, Ioanna Alexopoulou
Publikováno v:
ChemInform. 46
A highly efficient one-pot transformation of readily accessible furans into 4-hydroxy-2-cyclopentenones in H2O, using singlet oxygen as oxidant, has been developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8de788277e7899ce575de2cf36ce58ca
https://doi.org/10.1002/chin.201517079
https://doi.org/10.1002/chin.201517079
Autor:
Dimitris Kalaitzakis, Konstantinos Daskalakis, Myron Triantafyllakis, Manolis Sofiadis, Georgios Vassilikogiannakis
Publikováno v:
Organic Letters; Jul2019, Vol. 21 Issue 14, p5467-5470, 4p
Autor:
Tamsyn Montagnon, Myron Triantafyllakis, Georgios Vassilikogiannakis, Dimitris Kalaitzakis, Manolis Stratakis
Publikováno v:
ChemInform. 46
The purpose of this article is to give a taste of just how powerful the union between furans and photochemically-generated singlet oxygen is proving to be as a synthetic tool and to suggest that this chemistry is only now really coming of age. In att
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa96dd4956095a8ea906658ccfe3859a
https://doi.org/10.1002/chin.201505239
https://doi.org/10.1002/chin.201505239