Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Mokgethwa, B."'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1668-1692 (2018)
Sulfur-containing natural products are ubiquitous in nature, their most abundant source being marine organisms since sulfur, in the form of the sulfate ion, is the second most abundant anion in sea water after chloride. As part of natural products, s
Externí odkaz:
https://doaj.org/article/0bb0a6be41fd49ffbadfba4a61eb68b4
Autor:
Mulokwe, Pfanelo1 (AUTHOR), Marakalala, Mokgethwa B.1 (AUTHOR), Mabasa, Tommy F.1 (AUTHOR), Kinfe, Henok H.1 (AUTHOR) hhkinfe@uj.ac.za
Publikováno v:
Synthetic Communications. Dec2017, Vol. 47 Issue 24, p2352-2359. 8p.
Autor:
Marakalala, Mokgethwa B.1, Kinfe, Henok H.1 hhkinfe@uj.ac.za
Publikováno v:
European Journal of Organic Chemistry. 6/23/2017, Vol. 2017 Issue 23, p3311-3317. 7p. 6 Diagrams, 2 Charts.
Publikováno v:
European Journal of Organic Chemistry. 2017:3311-3317
Molecular iodine and diacetoxyiodobenzene promoted novel multicomponent methodology for the synthesis of (E)-1,3-diphenyl-1-butene derivatives is developed using styrene and thiophenol as substrates. The attractiveness of the protocol is its ability
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1668-1692 (2018)
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1668-1692 (2018)
Sulfur-containing natural products are ubiquitous in nature, their most abundant source being marine organisms since sulfur, in the form of the sulfate ion, is the second most abundant anion in sea water after chloride. As part of natural products, s
NaHSO4 supported on silica gel catalyses the aza-Diels-Alder reaction of o-hydroxybenzaldimines with 2,3-dihydrofuran to provide furanobenzopyrans in reasonable yields and diastereoselectivity. The catalyst is recyclable and reusable up to two times
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11e649678cdb8c9e06e1510e786dfc98
NaHSO4 supported on silica gel catalyzes the aza-Diels–Alder reaction of o-hydroxybenzaldimines with 2,3-dihydrofuran to provide furanobenzopyrans in reasonable yields and diastereoselectivity. The catalyst is recyclable and reusable up to two time
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62158134f9684e0780551f5de0f46169
Akademický článek
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Akademický článek
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Publikováno v:
European Journal of Organic Chemistry. 2017:3301-3301