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The Role of Metals and Ligands in Organic Hydroformylation, by Luca Gonsalvi, Antonella Guerriero, Eric Monflier, Frédéric Hapiot, Maurizio Peruzzini.Hydroformylation in Aqueous Biphasic Media Assisted by Molecular Receptors, by Frédéric Hapiot, Hervé Bricout, Sébastien Tilloy, Eric Monflier.Asymmetric Hydroformylation, by Bernabé F. Perandones, Cyril Godard, Carmen Claver.Domino Reactions Triggered by Hydroformylation, by Elena Petricci, Elena Cini.Rhodium-Catalyzed Hydroformylation in Fused Azapolycycles Synthesis, by Roberta Settambolo.Hydroformylation in Natural Product Synthesis, by Roderick W. Bates, Sivarajan Kasinathan.

The selective formation of bondings between molecules is one of the major challenges in organic chemistry, and the so-called aldol reaction is one of the most important for this purpose. These reactions are a highly useful tool for developing such novel substances as natural products and pharmaceuticals. Likes its highly successful and much appreciated predecessor,'Modern Aldol Reactions', this ready reference provides a systematic overview of methodologies for installing a required configuration during an aldol addition step, but shifts the focus so as to cover the latest developments. As such, it presents a set of brand new tools, including vinylogous Mukaiyama-aldol reactions and substrate-controlled aldol reactions, as well as asymmetric induction in aldol additions. Furthermore, new developments in existing stereoselective aldol additions are described, such as the deployment of supersilyl groups or organocatalyzed aldol additions. All of these methodologies are presented in the context of their deployment in the total synthesis of natural products.

In this book, the authors present topical research in the study of aldehydes. Topics discussed in this compilation include the synthesis and properties of intermediates in reactions of aldehydes with P(III) chlorides; synthesis of heterocyclic compounds by interaction of aldehydes with monoterpenoids; update on aliphatic aldehydes in lipid foods; inhibition of microbial biocatalysts by biomass-derived aldehydes and methods for engineering tolerance; co-oxidation processes promoted by N-hydroxyphthalimide/aldehyde systems; and the structure of gossypol condensation bis-product with 2-amino-4,6-dioxypyrimidine in acidic environment.

Chapter 1 - Aldehyde Chapter 2 - Formaldehyde Chapter 3 - Acetaldehyde Chapter 4 - Benzaldehyde and Cinnamaldehyde Chapter 5 - Hydroformylation Chapter 6 - Wittig Reaction Chapter 7 - Johnson-Corey-Chaykovsky Reaction Chapter 8 - Phenolic Aldehyde Chapter 9 - Ozonolysis and Nef Reaction Chapter 10 - Gossypol and Hydroxymethylfurfural Chapter 11 - Carbonylation, Hydroacylation and Takai Olefination Chapter 12 - Zincke and Organic Redox Reaction

Chapter 1 - Alkali Metal Chapter 2 - Lithium Chapter 3 - Sodium Chapter 4 - Potassium Chapter 5 - Rubidium Chapter 6 - Alkaline Earth Metal Chapter 7 - Beryllium Chapter 8 - Magnesium Chapter 9 - Calcium Chapter 10 - Strontium Chapter 11 - Barium

The aim of this book is to help people performing routine operations in Organic Synthesis in a laboratory. This book, the first one in a series, focuses on the oxidation of alcohols to aldehydes and ketones. Probably, this is the most important routine operation in Organic Synthesis.