ChemInform Abstract: Guanidine-Catalyzed [gamma]-Selective Morita--Baylis--Hillman Reactions on [alpha],[gamma]-Dialkyl-allenoates: Access to Densely Substituted Heterocycles

ChemInform Abstract: Guanidine-Catalyzed [gamma]-Selective Morita--Baylis--Hillman Reactions on [alpha],[gamma]-Dialkyl-allenoates: Access to Densely Substituted Heterocycles

The bicyclic guanidine MTBD is shown to be an efficient catalyst for the Morita--Baylis--Hillman reaction of allenoates (I) with aldehydes (II). [PUBLICATION ABSTRACT]

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Veröffentlicht in:ChemInform 2014-05, Vol.45 (19)
Hauptverfasser: Selig, Philipp, Turockin, Aleksej, Raven, William
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container_issue 19
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container_title ChemInform
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creator Selig, Philipp
Turockin, Aleksej
Raven, William
description The bicyclic guanidine MTBD is shown to be an efficient catalyst for the Morita--Baylis--Hillman reaction of allenoates (I) with aldehydes (II). [PUBLICATION ABSTRACT]
doi_str_mv 10.1002/chin.201419143
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title ChemInform Abstract: Guanidine-Catalyzed [gamma]-Selective Morita--Baylis--Hillman Reactions on [alpha],[gamma]-Dialkyl-allenoates: Access to Densely Substituted Heterocycles
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