Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Jean-Christophe Poupon"'
Publikováno v:
Angewandte Chemie. 118:1443-1448
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bd7bc855b2d4e1d75c6d6058693569d
https://doi.org/10.1002/ange.200503599
https://doi.org/10.1002/ange.200503599
Publikováno v:
ChemInform. 28
N -Boc amino ethers 1a–e when treated with allyltrialkylsilanes in the presence of TiCl4 afford the expected allylation compounds 2a–e and/or the unprecedented silylated oxazinones 3a–e or 4a–e.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7571d4a38cb13abf5ffcf05fe56d5b3
https://doi.org/10.1002/chin.199749175
https://doi.org/10.1002/chin.199749175
Publikováno v:
ChemInform. 41
Tetraarylphosphonium (TAP)-supported DMSO, TEMPO, and DIB reagents were synthesized and used for the oxidation of alcohols, including Swern oxidation and for the α-acetoxylation of ketones. By taking advantage of the predictable solubility propertie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a2d4d3a75461e88ab06b01abcea4c35
https://doi.org/10.1002/chin.201013040
https://doi.org/10.1002/chin.201013040
Publikováno v:
The Journal of organic chemistry. 74(22)
Tetraarylphosphonium (TAP)-supported DMSO, TEMPO, and DIB reagents were synthesized and used for the oxidation of alcohols, including Swern oxidation and for the alpha-acetoxylation of ketones. By taking advantage of the predictable solubility proper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfb2cf716e0a57c0c6a09a606429828c
https://pubmed.ncbi.nlm.nih.gov/19856924
https://pubmed.ncbi.nlm.nih.gov/19856924
Publikováno v:
The Journal of organic chemistry. 73(7)
New tetraarylphosphonium (TAP)-supported alkyl- and arylcarbodiimides were synthesized and used as coupling reagents for esterification reactions, amidation reactions and dehydration reactions of hydroxyesters. Taking advantage of the solubility prop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0125801858e30a24b78d58e186942bf
https://pubmed.ncbi.nlm.nih.gov/18315003
https://pubmed.ncbi.nlm.nih.gov/18315003
Publikováno v:
Organic letters. 9(18)
Phosphonium-supported tin reagents and catalysts were prepared and were shown to be effective in Stille couplings, radical dehalogenations, radical cyclizations, and carbonyl allylations. Not only could the tin residues be removed from the crude reac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78c67a844df79c350f648eacaf87f911
https://pubmed.ncbi.nlm.nih.gov/17672475
https://pubmed.ncbi.nlm.nih.gov/17672475
Publikováno v:
Angewandte Chemie (International ed. in English). 46(26)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b3ec82d7284d4812bba48fe8cab4a08
https://pubmed.ncbi.nlm.nih.gov/17516601
https://pubmed.ncbi.nlm.nih.gov/17516601
Publikováno v:
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2005, pas, pp.644. ⟨10.1055/s-2004-837294⟩
SYNTHESIS, Georg Thieme Verlag, 2005, pas, pp.644. ⟨10.1055/s-2004-837294⟩
Studies dealing with the diastereoselective installation of nine stereogenic centers of the C-12-C-25 subunit of bafilomycin A 1 1 are described. A spiroketal precursor has been chosen as a rigid scaffold owing to the central spiro center, the config
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75974a2924ecfe8d22b23409a7036cc6
https://hal.archives-ouvertes.fr/hal-00091469
https://hal.archives-ouvertes.fr/hal-00091469
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2003, 68 (12), pp.4700-4707. ⟨10.1021/jo034018e⟩
Journal of Organic Chemistry, American Chemical Society, 2003, 68 (12), pp.4700-4707. ⟨10.1021/jo034018e⟩
International audience; The synthesis of the C1-C11 fragment 33 of bafilomycin A1 was achieved. Intermediate ketone 16 was prepared in six steps from 4-oxopimelate 13. Desymmetrization of this ketone using Koga's chiral base followed by TMSCl quench
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76215583d184ce9842d3c3b705fac9c5
https://hal-polytechnique.archives-ouvertes.fr/hal-00954829
https://hal-polytechnique.archives-ouvertes.fr/hal-00954829
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2002, 67 (7), pp.2118-2124. ⟨10.1021/jo016231l⟩
Journal of Organic Chemistry, American Chemical Society, 2002, 67 (7), pp.2118-2124. ⟨10.1021/jo016231l⟩
International audience; Current efforts devoted to the synthesis of Bafilomycin A1 led us to investigate a synthetic route through a spiroketal intermediate for the construction of the C15-C25 subunit. Preliminary studies for the diastereoselective i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4cf08de12b47f5da9c1267e66906fb4
https://pubmed.ncbi.nlm.nih.gov/11925217
https://pubmed.ncbi.nlm.nih.gov/11925217