Cyclic 1‐Azadienes in the Organocatalytic Inverse‐Electron‐Demand Aza‐Diels‐Alder Cycloadditions | Zendy

Skrzyńska Anna | Zendy; Frankowski Sebastian | Zendy; Albrecht Łukasz | Zendy

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Cyclic 1‐Azadienes in the Organocatalytic Inverse‐Electron‐Demand Aza‐Diels‐Alder Cycloadditions

Author(s) -

Skrzyńska Anna,

Frankowski Sebastian,

Albrecht Łukasz

Publication year - 2020

Publication title -

asian journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.846

H-Index - 44

eISSN - 2193-5815

pISSN - 2193-5807

DOI - 10.1002/ajoc.202000332

Subject(s) - cycloaddition , chemistry , organocatalysis , diels–alder reaction , inverse , combinatorial chemistry , enantioselective synthesis , catalysis , organic chemistry , mathematics , geometry

The inverse‐electron‐demand hetero‐Diels‐Alder (IEDHDA) reaction constitutes a useful and highly reliable method for the construction of various heterocycles. In the manuscript, a recent progress in the organocatalytic IEDHDA cycloaddition using cyclic 1‐azadienes as hetero‐dienes has been summarized and discussed. Since 2010 many interesting, new reactions involving these substrates have been identified and developed. They are based on various organocatalytic activation modes providing access to valuable nitrogen‐heterocycles. Excellent stereochemical reliability of asymmetric organocatalysis combined with the importance of the structural motifs obtained as a result of the cycloaddition makes these strategies highly relevant for the contemporary organic synthesis.

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