A review. After more than 125 yr, the Friedel-Crafts alkylation is still one of the most studied and most utilized reactions in org. synthesis. What is the secret of this astonishing success Perhaps the great versatility in; scope and applicability continues to justify its crucial role in the synthesis of more and more complex mols. However, it has taken more than a century for asym. catalytic versions of this reaction to be developed and subsequently extended to a range of arom. compds. and alkylating agents. Herein recent developments in the design and use of catalytic and stereoselective strategies for the alkylation of arom. systems and synthesis of a wide range of polyfunctionalized enantiomerically enriched compds. were reviewed.

M. BANDINI, A. MELLONI, UMANI RONCHI A. (2004). New Catalytic Approaches in the Enantioselective Friedel-Crafts Alkylation Reaction. ANGEWANDTE CHEMIE. INTERNATIONAL EDITION, 43, 550-556 [10.1002/anie.200301679].

New Catalytic Approaches in the Enantioselective Friedel-Crafts Alkylation Reaction

BANDINI, MARCO;MELLONI, ALFONSO;UMANI RONCHI, ACHILLE
2004

Abstract

A review. After more than 125 yr, the Friedel-Crafts alkylation is still one of the most studied and most utilized reactions in org. synthesis. What is the secret of this astonishing success Perhaps the great versatility in; scope and applicability continues to justify its crucial role in the synthesis of more and more complex mols. However, it has taken more than a century for asym. catalytic versions of this reaction to be developed and subsequently extended to a range of arom. compds. and alkylating agents. Herein recent developments in the design and use of catalytic and stereoselective strategies for the alkylation of arom. systems and synthesis of a wide range of polyfunctionalized enantiomerically enriched compds. were reviewed.
2004
M. BANDINI, A. MELLONI, UMANI RONCHI A. (2004). New Catalytic Approaches in the Enantioselective Friedel-Crafts Alkylation Reaction. ANGEWANDTE CHEMIE. INTERNATIONAL EDITION, 43, 550-556 [10.1002/anie.200301679].
M. BANDINI; A. MELLONI; UMANI RONCHI A.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/1854
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