P
Pier Giorgio Cozzi
Researcher at University of Bologna
Publications - 290
Citations - 9660
Pier Giorgio Cozzi is an academic researcher from University of Bologna. The author has contributed to research in topics: Enantioselective synthesis & Catalysis. The author has an hindex of 46, co-authored 277 publications receiving 8695 citations. Previous affiliations of Pier Giorgio Cozzi include University College Dublin & RWTH Aachen University.
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Metal–Salen Schiff base complexes in catalysis: practical aspects
TL;DR: Practical guidelines for the preparation and use of different Schiff base metal complexes in the field of catalytic transformations are discussed in this tutorial review.
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Enantioselective Catalytic Formation of Quaternary Stereogenic Centers
TL;DR: In this article, the authors discuss recent highlights of this new direction in catalysis research: the formation of quaternary stereogenic centers by enantioselective catalytic methodologies.
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Direct Nucleophilic SN1‐Type Reactions of Alcohols
Enrico Emer,Riccardo Sinisi,Montse Guiteras Capdevila,Diego Petruzziello,Francesco De Vincentiis,Pier Giorgio Cozzi +5 more
TL;DR: A review of the approaches leading to a greener process are examined in detail, and the advances achieved to date in this important transformation are presented in this article, where a list of key research areas including the direct nucleophilic reactions of alcohols is established.
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Acetylenes in Catalysis: Enantioselective Additions to Carbonyl Groups and Imines and Applications Beyond
TL;DR: An overview of recent results in these areas can be found in this paper, where a considerable number of publications have appeared that focus on the enantioselective addition of acetylenes to carbonyls and imines.
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Sequential One-Pot InBr3-Catalyzed 1,4- then 1,2-Nucleophilic Addition to Enones
Marco Bandini,Pier Giorgio Cozzi,Massimo Giacomini,Paolo Melchiorre,Simona Selva,Achille Umani‐Ronchi +5 more
TL;DR: With the optimized atom-efficient protocol, several polyfunctionalized alpha-silyloxy cyanohydrins were synthesized in good to excellent yields and a notable level of simple 1,3-diastereoselection was recorded in the case of 2-cyclohexen-1-one 2c.