Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Daniel Laurich"'
Publikováno v:
Chemistry - A European Journal. 22:237-247
3-Oxo-5-alkynoic acid esters, on treatment with a carbophilic catalyst, undergo 6-endo-dig cyclization reactions to furnish either 2-pyrones or 4-pyrones in high yields. The regiochemical course can be dialed in by the proper choice of the alcohol pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6745450436fe289c75dd742f080e76de
https://doi.org/10.1002/chem.201503403
https://doi.org/10.1002/chem.201503403
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6cf7dd136b984b82cd7c78fcc6c47a58
https://doi.org/10.1002/chin.201621040
https://doi.org/10.1002/chin.201621040
Autor:
Louis Morency, Vilnis Liepins, Daniel Laurich, Jaques-Alexis Funel, Laure C. Bouchez, Minoru Tamiya, Florent Beaufils, Ryan Gilmour, François-Hugues Porée, Alois Fürstner
Publikováno v:
Chemistry - A European Journal. 15:3983-4010
Nature is a pretty unselective "chemist" when it comes to making the highly cytotoxic amphidinolide macrolides of the B/G/H series. To date, 16 different such compounds have been isolated, all of which could now be approached by a highly convergent a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c0324ec47ffeaa3f6116712720e5375
https://doi.org/10.1002/chem.200802067
https://doi.org/10.1002/chem.200802067
Autor:
Vilnis Liepins, Laure C. Bouchez, François-Hugues Porée, Minoru Tamiya, Daniel Laurich, Florent Beaufils, Ryan Gilmour, Jacques-Alexis Funel, Alois Fuerstner
Publikováno v:
ChemInform. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b40e2eb40ca5ba9181446d53b40fc252
https://doi.org/10.1002/chin.200816208
https://doi.org/10.1002/chin.200816208
Autor:
Alois Fürstner, Vilnis Liepins, Daniel Laurich, Laure C. Bouchez, Minoru Tamiya, Jacques-Alexis Funel, François-Hugues Porée, Florent Beaufils, Ryan Gilmour
Publikováno v:
Angewandte Chemie (International ed. in English). 46(48)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d59448acbe80a787cf763ef5d88b384
https://pubmed.ncbi.nlm.nih.gov/17969211
https://pubmed.ncbi.nlm.nih.gov/17969211
Publikováno v:
ChemInform. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d074ee56a401527f189535efe1091e2e
https://doi.org/10.1002/chin.200438089
https://doi.org/10.1002/chin.200438089
Publikováno v:
The Journal of organic chemistry. 69(11)
A chemo- and regioselective cross-coupling reaction of the functionalized aryl triflate 5 with octylmagnesium bromide catalyzed by cheap, nontoxic, and environmentally benign Fe(acac)(3) sets the basis for a practical and scaleable synthesis of the o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1da574e0927a1dc422f45da9f2fdb6e
https://pubmed.ncbi.nlm.nih.gov/15153030
https://pubmed.ncbi.nlm.nih.gov/15153030
Autor:
François-Hugues Porée, Minoru Tamiya, Laure C. Bouchez, Jaques-Alexis Funel, Florent Beaufils, Ryan Gilmour, Alois Fürstner, Vilnis Liepins, Daniel Laurich, Louis Morency
Publikováno v:
Chemistry - A European Journal. 15:3907-3907
Highly cytotoxic amphidinolide macrolides have been prepared in a highly convergent and largely catalysis-based route. In their Full Paper on page 3983 ff., and two subsequent papers, A. Furstner et al. describe the total synthesis and biological eva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c858f83133b90f2a583835dbe97cedf6
https://doi.org/10.1002/chem.200990053
https://doi.org/10.1002/chem.200990053
Publikováno v:
Organic Syntheses
Organic Syntheses : An annual publication of satisfactory methods for the preparation of organic chemicals
Organic Syntheses : An annual publication of satisfactory methods for the preparation of organic chemicals, J. Wiley & Sons, 2006, 83, pp.103. ⟨10.15227/orgsyn.083.0103⟩
Organic Syntheses : An annual publication of satisfactory methods for the preparation of organic chemicals
Organic Syntheses : An annual publication of satisfactory methods for the preparation of organic chemicals, J. Wiley & Sons, 2006, 83, pp.103. ⟨10.15227/orgsyn.083.0103⟩
2-Iodoaniline 2,5-Dimethoxytetrahydrofuran 1-(2-Iodophenyl)pyrrole 1-(2-(1-Propynyl)phenyl)pyrrole Palladium, dichlorobis(triphenylphosphine)- 4-Methylpyrrolo[1,2a]quinoline Indium chloride Keywords: indium; catalyst; cycloisomerization; methylpyrrol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bb28ff04ef035027a44d363a9df0c6e
https://doi.org/10.15227/orgsyn.083.0103
https://doi.org/10.15227/orgsyn.083.0103