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Inside Cover: Enantioselective Organocatalytic Four‐Atom Ring Expansion of Cyclobutanones: Synthesis of Benzazocinones (Angew. Chem. Int. Ed. 2/2019)
Author(s) -
Zhou Yirong,
Wei YunLong,
Rodriguez Jean,
Coquerel Yoann
Publication year - 2019
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201813897
Subject(s) - enantioselective synthesis , ring (chemistry) , organocatalysis , nitrogen atom , chemistry , cover (algebra) , atom (system on chip) , stereochemistry , catalysis , organic chemistry , computer science , engineering , mechanical engineering , embedded system
In the footsteps of Count Monte Cristo escaping the Château d'If fortress on the way to his treasure, French and Chinese chemists collaboratively elaborated an enantioselective organocatalytic four‐atom ring‐expansion / two‐atom ring‐contraction synthetic strategy to reach rare eight‐ and six‐membered nitrogen heterocycles. The chemistry is described by J. Rodriguez, Y. Coquerel and co‐workers in their Communication on page 456 ff.