Protocols for building an organic chemical ontology

in International Journal of Knowledge and Learning (2008), 4(2/3), 152-175

We will describe the different stages involved in the collaborative construction of an organic chemical ontology by chemists. We will disclose our experience, as chemists, in learning, how to build a ... [more ▼]

We will describe the different stages involved in the collaborative construction of an organic chemical ontology by chemists. We will disclose our experience, as chemists, in learning, how to build a collaborative ontology and how to use the ontology software from that of an artificial intelligence scientist. We will then disclose our work in developing the protocols to work within the community of chemists to build a collaborative ontology. Useful perceptions about the use of the ontology will also be discussed. [less ▲]

EnCOrE : Encyclopédie de Chimie Organique Electronique

Poster (2006, December)

EnCOrE (Encyclopédie de Chimie Organique Electronique): An Original Way to Represent and Transfer Knowledge from Freshmen to Researchers in Organic Chemistry

in Ritrovato, Pierluigi; Cerri, Stefano A.; Salerno, Saverio (Eds.) et al Towards the Learning Grid Advances in Human Learning Services (2005)

EnCOrE is an original proposal which is expected to allow the sharing and the transfer of knowledge in organic chemistry. The system will use MIDES software, whith a peer-to-peer architecture, which will ... [more ▼]

EnCOrE is an original proposal which is expected to allow the sharing and the transfer of knowledge in organic chemistry. The system will use MIDES software, whith a peer-to-peer architecture, which will allow setting up a technological and methodological frame to allow collaborative building of knowledge in between chemists. Learning Grid's services will help for Experimental Electronic Laboratory “LabCOrE” as well as for predictive computational tools. [less ▲]

Osmium (VI) – selenoxyde and selenide – osmium (VIII) : A Perfect Couple of Reagents

Poster (2001, December)

Osmium (VI) – selenoxyde : A Perfect Couple of Reagents

Poster (2001, July)

Powerful Alternative Asymmetric Catalytic Dihydroxylation of Olefins

Poster (2000, November)

Catalytic asymmetric dihydroxylation of alpha-methylstyrene by air

in Tetrahedron Letters (1999), 40(22), 4189-4192

Dioxygen is able, under visible irradiation, to promote the high yielding and highly asymmetric dihydroxylation of alpha-methylstyrene in the presence of catalytic amounts of Os(VI), phthalazine ... [more ▼]

Dioxygen is able, under visible irradiation, to promote the high yielding and highly asymmetric dihydroxylation of alpha-methylstyrene in the presence of catalytic amounts of Os(VI), phthalazine dihydroquinidine chiral ligand [(DHQD)(2)PHAL]. (C) 1999 Published by Elsevier Science Ltd. Ail rights reserved. [less ▲]

Powerful alternative asymmetric Catalytic dihydroxylation of olefins

Poster (1998, November)

Oxidation of allylselenides with the Sharpless AD reagents

Poster (1998, July)

Oxidation of allylselenides with the Sharpless AD-reagents

in Tetrahedron Letters (1997), 38(18), 3315-3318

Allylselenides are efficiently oxidized by AD-mix reagents. Oxidation takes chemoselectively place on the selenium atom of allylselenides bearing a methylseleno or a phenylseleno moiety, but ... [more ▼]

Allylselenides are efficiently oxidized by AD-mix reagents. Oxidation takes chemoselectively place on the selenium atom of allylselenides bearing a methylseleno or a phenylseleno moiety, but chemoselectively occurs on the C,C double bond of the corresponding o-nitrophenyl derivatives. [less ▲]