Organic Synthesis and methodologies
Pd, Ru, Rh, Ir-catalaysis, Pincer complexes Catalysis, Homo & Heterogenous Catalysis,
Pd, Ru, Rh, Ir-catalaysis, Pincer complexes Catalysis, Homo & Heterogenous Catalysis,
Named Reactions and others:
Named Reactions and others:
Susuki, Sonogashira, Heck, Buchwald, Kumada, Negishi, Stille coupling reactionsFriedlander reaction, Pfzinger reaction, Fischer indole réaction, Barbier reaction, Mannich reaction, Michael, Ulmann, Pictet Spengler, Grignard reactions, Chan Lam reaction, Baylis Hilman reaction, Kabbe condensation, Aza- Diels alder, reduction, oxidation, condensation, cyclisation, moisture sensitive, allylations, N-arylations, periodate oxidations, sodium borohydride reductions, Diels alder reaction, Phase transfer reactions, 1,3-dipolar cycloadditions,
Susuki, Sonogashira, Heck, Buchwald, Kumada, Negishi, Stille coupling reactionsFriedlander reaction, Pfzinger reaction, Fischer indole réaction, Barbier reaction, Mannich reaction, Michael, Ulmann, Pictet Spengler, Grignard reactions, Chan Lam reaction, Baylis Hilman reaction, Kabbe condensation, Aza- Diels alder, reduction, oxidation, condensation, cyclisation, moisture sensitive, allylations, N-arylations, periodate oxidations, sodium borohydride reductions, Diels alder reaction, Phase transfer reactions, 1,3-dipolar cycloadditions,
Heterocyclics
Heterocyclics
Isocoumarins, Isocarbostyrils, isoquinolinone, quinolinones, isoquinolines, quinolines, naphthyridines, xanthenes, xanthenediones, acridindiones, quinazolines, thiazoles, pyrazoles, triazoles, thiadiazoles, oxazoles,etc. and the S, Se, Te analogues
Isocoumarins, Isocarbostyrils, isoquinolinone, quinolinones, isoquinolines, quinolines, naphthyridines, xanthenes, xanthenediones, acridindiones, quinazolines, thiazoles, pyrazoles, triazoles, thiadiazoles, oxazoles,etc. and the S, Se, Te analogues
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