Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Louis Hamon"'
Neue Übersetzung ins Deutsche: Die Handlesekunst ist die Praxis der Wahrsagerei durch das Studium der Handfläche. Sie wird auch als Handlesen, Chiromantie, Chirologie oder Cheirologie bezeichnet und ist in der ganzen Welt verbreitet, wobei es zahlr
Autor:
Louis Hamon, Corinne Vanucci-Bacqué, Catherine Kadouri-Puchot, Gérard Lhommet, Virginie Mouriès-Mansuy, Valerie Toum, Luc Dechoux
Publikováno v:
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2011, 2011 (17), pp.2781-2788. ⟨10.1055/s-0030-1260132⟩
Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, 2011, 2011 (17), pp.2781-2788. ⟨10.1055/s-0030-1260132⟩
SYNTHESIS, Georg Thieme Verlag, 2011, 2011 (17), pp.2781-2788. ⟨10.1055/s-0030-1260132⟩
Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, 2011, 2011 (17), pp.2781-2788. ⟨10.1055/s-0030-1260132⟩
Bromocyclization of diesters (I) and (VI) affords furanone structures bearing one ester function.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f12bf74db97ccb5e87f20160da1fec69
https://doi.org/10.1055/s-0030-1260132
https://doi.org/10.1055/s-0030-1260132
Autor:
Louis Hamon, Andrée Parlier, Henri Rudler, Sandra Beaupierre, Patrick Herson, Catherine Kadouri-Puchot, Nathalie Jarosz, Jean-Claude Daran
Publikováno v:
Tetrahedron Letters. 50:7274-7279
In contrast to substituted 4-acetic acid 1,4-dihydropyridines, giving only δ-lactones upon intramolecular reactions, 2-substituted 1,2-dihydropyridines led, besides to δ-lactones, also to new, structurally interesting γ-lactones as the result of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa081d1ce33774767b254f608b954bf6
https://doi.org/10.1016/j.tetlet.2009.10.038
https://doi.org/10.1016/j.tetlet.2009.10.038
Autor:
Jean-Claude Daran, Patrick Herson, Louis Hamon, Patrick Chaquin, Andrée Parlier, Henri Rudler
Publikováno v:
Tetrahedron. 65:5552-5562
The interaction of bis(trimethylsilyl)ketene acetals with various pyridines provides a direct, general, diastereoselective access to fluorolactones via the formation of dihydropyridine-substituted carboxylic acids. These in turn reacted with selectfl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35ddaea622b7e42f879a0623a8005fb1
https://doi.org/10.1016/j.tet.2009.02.086
https://doi.org/10.1016/j.tet.2009.02.086
Publikováno v:
European Journal of Mass Spectrometry. 14:61-69
The affinity of cyclic oligomers of sugar amino acid and sugar-aza-crown ether compounds towards various transition metal cations (CuII, NiII, CoII, FeII and ZnII) was investigated with positive-ion electrospray mass spectrometry. The binding between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35e5cbd6e6204aaac671a33a1d9c123d
https://doi.org/10.1255/ejms.912
https://doi.org/10.1255/ejms.912
Autor:
Louis Hamon, Hodney Lubin, Emilie Banide, Catherine Kadouri-Puchot, Luc Dechoux, Vincent Lemau de Talance, Sébastien Comesse, Gregory Schmidt
Publikováno v:
European Journal of Organic Chemistry. 2007:4517-4524
β-Amino alcohols with an (E)-vinylsilane moiety were cyclized in the presence of N-bromosuccinimide to afford diastereomerically pure azetidines. The chemo- and stereoselectivities of this bromocyclization are discussed. AM1 calculations support the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae419470493426868cf694fb72bf3a48
https://doi.org/10.1002/ejoc.200700283
https://doi.org/10.1002/ejoc.200700283
Publikováno v:
Carbohydrate Research. 338:1591-1601
The synthesis of polyfunctionalized δ-lactams as key intermediates of glycomimetics in the 2-acetamido-2-deoxy sugar series is presented. Starting from a chiral γ-amino vinylic ester synthesized from Garner's aldehyde and after regioselective reduc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26e9a94d289988bb4562e0239d592e3a
https://doi.org/10.1016/s0008-6215(03)00239-8
https://doi.org/10.1016/s0008-6215(03)00239-8
Publikováno v:
Synthesis. 2003:0859-0862
A series of polysubstituted pyrroles 3 have been synthesized efficiently in two or three steps starting from primary amines 1. The key step of this process is the bromocyclization of δ-dienamino esters 2. The chemoselectivity of this reaction is dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2ea92606336d1241e80209448c8e5cd
https://doi.org/10.1055/s-2003-38690
https://doi.org/10.1055/s-2003-38690
Publikováno v:
European Journal of Organic Chemistry. 2002:736-744
As an approach to the synthesis of amiclenomycin (1), we describe here the synthesis of a 1-aminocyclohexa-2,5-diene moiety. The cis isomer 2 was obtained by means of a Diels− Alder reaction between trans-1,2-bis(phenylsulfonyl)ethylene and N-(ally
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4ba0dd25590e16aa5ad69b1a5682e27
https://doi.org/10.1002/1099-0690(200202)2002:4<736::aid-ejoc736>3.0.co
https://doi.org/10.1002/1099-0690(200202)2002:4<736::aid-ejoc736>3.0.co
Publikováno v:
European Journal of Organic Chemistry. 2000:155-163
Two strategies have been explored to build the highly strained eleven-membered ring 2, a potential precursor for the biosynthetic key intermediate of the protoilludane family: an intramolecular Horner-Wadsworth-Emmons olefination and an intramolecula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ca265162420d4bc4a09ed7e2a42683d
https://doi.org/10.1002/(sici)1099-0690(200001)2000:1<155::aid-ejoc155>3.0.co
https://doi.org/10.1002/(sici)1099-0690(200001)2000:1<155::aid-ejoc155>3.0.co