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The Baylis-Hillman reaction: A strategy for the preparation of multi-functionalised intermediates for organic synthesis.
(Soc Brasileira QuimicaSao PauloBrasil, 2000)
Bronsted Acid Catalyzed Morita-Baylis-Hillman Reaction: A New Mechanistic View for Thioureas Revealed by ESI-MS(/MS) Monitoring and DFT Calculations
(Wiley-v C H Verlag Gmbh, 2009-01-01)
A Morita-Baylis-Hillman (MBH) reaction catalyzed by thiourea was monitored by ESI-MS(/MS) and key intermediates were intercepted and characterized. These intermediates Suggest that thiourea acts as an organocatalyst in all ...
Bronsted Acid Catalyzed Morita-Baylis-Hillman Reaction: A New Mechanistic View for Thioureas Revealed by ESI-MS(/MS) Monitoring and DFT Calculations
(Wiley-v C H Verlag Gmbh, 2009-01-01)
A Morita-Baylis-Hillman (MBH) reaction catalyzed by thiourea was monitored by ESI-MS(/MS) and key intermediates were intercepted and characterized. These intermediates Suggest that thiourea acts as an organocatalyst in all ...
Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts
(PERGAMON-ELSEVIER SCIENCE LTDOXFORD, 2012)
Chalcogenolate mediated Michael-aldol cascade reactions consists of a very efficient route to multi-functionalized gamma-hydroxichalcogenides. Although, when selenolates are employed, these gamma-hydroxichalcogenides can ...