Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Blennolide C"'
Publikováno v:
ChemistrySelect. 2:3268-3275
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7387bd140aeb67af8c0b582062a6002
https://doi.org/10.1002/slct.201700667
https://doi.org/10.1002/slct.201700667
Publikováno v:
Advanced Synthesis & Catalysis. 357:3303-3308
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c30db401d9b8b7c60a1f619693f3900
https://doi.org/10.1002/adsc.201500524
https://doi.org/10.1002/adsc.201500524
Akademický článek
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Autor:
Carl Friedrich Nising, Arantxa Encinas, Emilie M. C. Singer, Martin Nieger, Hülya Sahin, Stefan Bräse, Anne C. Meister
Publikováno v:
European Journal of Organic Chemistry. 2014:4861-4875
Mycotoxins of the tetrahydroxanthone class of natural products possess a large number of interesting biological properties. In this full paper, we present our synthetic strategy to some members of this class of compounds, namely the blennolides A and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1052d4be2d88a64411d73903f5c29c4d
https://doi.org/10.1002/ejoc.201402083
https://doi.org/10.1002/ejoc.201402083
Publikováno v:
Org. Biomol. Chem.. 12:5601-5610
The first stereoselective total synthesis of gonytolide C, which is a monomeric unit of an innate immune promoter gonytolide A, has been accomplished from the aldol reaction between acetophenone derived from orcinol and butyrolactone containing α-ke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84478463ddd4217a5ab2ed672793e1e2
https://doi.org/10.1039/c4ob00950a
https://doi.org/10.1039/c4ob00950a
Autor:
Stefan Bräse, Emilie M. C. Gérard
Publikováno v:
Chemistry - A European Journal. 14:8086-8089
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94bfddc221174a884a3d8387768bf53d
https://doi.org/10.1002/chem.200801507
https://doi.org/10.1002/chem.200801507
Publikováno v:
ChemInform. 46
Key to the syntheses of blennolide C (I) and gonytolide C (II), is an enantioselective domino-Wacker/carbonylation/methoxylation reaction to set up the stereocenter at C-4a.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3f9be16e3d4769bb2674e0b63c4a46f
https://doi.org/10.1002/chin.201504227
https://doi.org/10.1002/chin.201504227
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 20(28)
The first enantioselective total syntheses of the tetrahydroxanthenone (-)-blennolide C (ent-4) and related γ-lactonyl chromanone (-)-gonytolide C (ent-3) are reported. Key to the syntheses is an enantioselective domino-Wacker/carbonylation/methoxyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae60f5ed5f979ab32fe4440617696110
https://pubmed.ncbi.nlm.nih.gov/24905446
https://pubmed.ncbi.nlm.nih.gov/24905446
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 19(33)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be898df17ee32a3f251e9415368f6a68
https://pubmed.ncbi.nlm.nih.gov/23828509
https://pubmed.ncbi.nlm.nih.gov/23828509
A concise approach to the tetrahydroxanthone natural products employing vinylogous addition of siloxyfurans to benzopyryliums and a late-stage Dieckmann cyclization has been developed. With this methodology, chiral, racemic forms of the natural produ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b199d1583949b106d5acb6cf5126202
https://europepmc.org/articles/PMC3099260/
https://europepmc.org/articles/PMC3099260/
