D
Daniel Beaupère
Researcher at University of Picardie Jules Verne
Publications - 91
Citations - 852
Daniel Beaupère is an academic researcher from University of Picardie Jules Verne. The author has contributed to research in topics: Catalysis & Yield (chemistry). The author has an hindex of 17, co-authored 91 publications receiving 832 citations.
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Journal ArticleDOI
Effects of phenolic compounds on Agrobacterium vir genes and gene transfer induction*/a plausible molecular mechanism of phenol binding protein activation
Philippe Joubert,Daniel Beaupère,Philippe Lelièvre,Anne Wadouachi,Rajbir S. Sangwan,Brigitte S. Sangwan-Norreel +5 more
TL;DR: It is confirmed that virulence induction and transformation rates are increased by the use of phenolic vir inducers bearing an unsaturated lateral chain, but it is found that the presence of at least one ortho-methoxy group in the phenolic compounds is required to increase the vir gene induction.
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A new and direct access to glycono-1,4-lactones from glycopyranoses by regioselective oxidation and subsequent ring restriction
TL;DR: In this article, the authors show that the treatment of partially protected or unprotected carbohydrates with the RhH(PPh 3 ) 4 -benzalacetone system leads exclusively to glycono-1,4-lactones by regioselective oxidation and subsequent ring restriction.
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One-pot stereoselective synthesis of glycosyl azides via 1,2-cyclic sulfite
TL;DR: In this article, treatment of partially protected or unprotected aldoses with N,N ′-thionyldiimidazole and then, lithium azide leads stereoselectively to glycosyl azides.
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A novel stereospecific synthesis of glycosyl cyanides from 1,2-O-sulfinyl derivatives.
TL;DR: An efficient synthesis of 1,2-trans-glycosyl cyanides via 1, 2-O-sulfinyl monosaccharides is described, which have a free hydroxyl group at C-2 ready for further modification.
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Direct Regioselective Chlorination of Unprotected Hexitols and Pentitols by Viehe's Salt
TL;DR: Viehe's salt allows the transformation of unprotected hexitols and pentitols into linear 1,6 and 1,5 dichloro derivatives in high yields.