Asymmetric Organocatalysis: From Infancy to Adolescence
Top Cited Papers
- 3 June 2008
- journal article
- review article
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 47 (25), 4638-4660
- https://doi.org/10.1002/anie.200704684
Abstract
After an initial period of validating asymmetric organocatalysis by using a wide range of important model reactions that constitute the essential tools of organic synthesis, the time has now been reached when organocatalysis can be used to address specific issues and solve pending problems of stereochemical relevance. This Review deals with selected studies reported in 2006 and the first half of 2007, and is intended to highlight four main aspects that may be taken as testimony of the present status and prospective of organocatalysis: a) chemical efficiency; b) discovery of new substrate combinations to give new asymmetric syntheses; c) development of new catalysts for specific purposes by using mechanistic findings; and d) applications of organocatalytic reactions in the asymmetric total synthesis of target natural products and known compounds of biological and pharmaceutical relevance.Keywords
This publication has 259 references indexed in Scilit:
- Chirale Brønsted‐Säuren in der katalytischen asymmetrischen Nazarov‐Reaktion – die erste enantioselektive organokatalytische elektrocyclische ReaktionAngewandte Chemie, 2007
- Combined Proline–Surfactant Organocatalyst for the Highly Diastereo- and Enantioselective Aqueous Direct Cross-Aldol Reaction of AldehydesAngewandte Chemie, 2006
- Functionalized Chiral Ionic Liquids as Highly Efficient Asymmetric Organocatalysts for Michael Addition to NitroolefinsAngewandte Chemie, 2006
- Asymmetric Organocatalytic Henry ReactionAngewandte Chemie, 2006
- Amino Acid‐Catalyzed Asymmetric Carbohydrate Formation: Organocatalytic One‐Step De Novo Synthesis of Keto and Amino SugarsAdvanced Synthesis & Catalysis, 2006
- The Origin of Stereoselectivity in Primary Amino Acid Catalyzed Intermolecular Aldol ReactionsAngewandte Chemie, 2005
- Design of an Axially Chiral Amino Acid with a Binaphthyl Backbone as an Organocatalyst for a Direct Asymmetric Aldol ReactionAngewandte Chemie International Edition, 2005
- Synthesis ofβ-Hydroxyaldehydes with Stereogenic Quaternary Carbon Centers by Direct Organocatalytic Asymmetric Aldol ReactionsAngewandte Chemie, 2004
- A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal AlkynesAngewandte Chemie International Edition, 2002
- Asymmetric Catalysis: Science and Opportunities (Nobel Lecture) Copyright© The Nobel Foundation 2002. We thank the Nobel Foundation, Stockholm, for permission to print this lecture.Angewandte Chemie International Edition, 2002