Design and Application of Chiral Sulfinyl Imine Ligands and Synthetic Applications of N-sulfinyl Metalloenamine-based Diastereoselective Reactions

Design and Application of Chiral Sulfinyl Imine Ligands and Synthetic Applications of N-sulfinyl Metalloenamine-based Diastereoselective Reactions
Title Design and Application of Chiral Sulfinyl Imine Ligands and Synthetic Applications of N-sulfinyl Metalloenamine-based Diastereoselective Reactions PDF eBook
Author Laurie Beth Schenkel
Publisher
Pages 424
Release 2005
Genre
ISBN

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The Design, Synthesis, and Utility of Sulfinyl Imine-based Ligands for Asymmetric Catalysis

The Design, Synthesis, and Utility of Sulfinyl Imine-based Ligands for Asymmetric Catalysis
Title The Design, Synthesis, and Utility of Sulfinyl Imine-based Ligands for Asymmetric Catalysis PDF eBook
Author Timothy Duncan Owens
Publisher
Pages 284
Release 2002
Genre
ISBN

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Dissertation Abstracts International

Dissertation Abstracts International
Title Dissertation Abstracts International PDF eBook
Author
Publisher
Pages 780
Release 2006
Genre Dissertations, Academic
ISBN

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Chiral Auxiliary Design and Application. Diastereoselective Ester Enolate Alkylations. Asymmetric Synthesis of Chiral Cyclohexanes. Synthesis and Characterization of N,N'-disubstituted Diaza-14- Crown-4 Ethers

Chiral Auxiliary Design and Application. Diastereoselective Ester Enolate Alkylations. Asymmetric Synthesis of Chiral Cyclohexanes. Synthesis and Characterization of N,N'-disubstituted Diaza-14- Crown-4 Ethers
Title Chiral Auxiliary Design and Application. Diastereoselective Ester Enolate Alkylations. Asymmetric Synthesis of Chiral Cyclohexanes. Synthesis and Characterization of N,N'-disubstituted Diaza-14- Crown-4 Ethers PDF eBook
Author Richard E. Taylor
Publisher
Pages 126
Release 1992
Genre
ISBN

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Chiral Sulfur Reagents

Chiral Sulfur Reagents
Title Chiral Sulfur Reagents PDF eBook
Author Marian Mikolajczyk
Publisher CRC Press
Pages 294
Release 1997-06-09
Genre Science
ISBN 9780849391200

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Over the last three decades, more than 40 different classes of chiral (mirror-image) sulfur compounds have been described, and a number of useful procedures and applications have been developed for their use. Emphasizing modern methodologies, Chiral Sulfur Reagents demonstrates the great potential of enantionmerically pure sulfur reagents in transmitting chirality to other centers. Each chapter highlights the synthesis and synthetic uses of a particular class of chiral sulfur reagent, followed by examples of the most important experimental procedures.

Organosulfur Chemistry in Asymmetric Synthesis

Organosulfur Chemistry in Asymmetric Synthesis
Title Organosulfur Chemistry in Asymmetric Synthesis PDF eBook
Author Takeshi Toru
Publisher John Wiley & Sons
Pages 448
Release 2008-09-08
Genre Science
ISBN 3527623248

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In this first book to gather the information on this hot topic otherwise widely spread throughout the literature, experienced editors and top international authors cover everything the reader needs -- from the synthesis of chiral organosulfur compounds to applications and catalysis: * Asymmetric synthesis of chiral sulfinates and sulfoxides * Synthesis and use of chiral dithioacetal derivatives, ylids, chiral sulfoximines and sulfinamides * Use of chiral sulfoxides as ligands in catalysis * Asymmetric reactions of alpha-sulfenyl, alpha-sulfinyl and alpha-sulfonyl carbanions. As a result, readers will be able to improve their own performance in asymmetric synthesis.

Domino Reactions in Organic Synthesis

Domino Reactions in Organic Synthesis
Title Domino Reactions in Organic Synthesis PDF eBook
Author Lutz F. Tietze
Publisher John Wiley & Sons
Pages 631
Release 2006-12-13
Genre Science
ISBN 3527608680

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Domino reactions enable you to build complex structures in one-pot reactions without the need to isolate intermediates- a dream comes true. In this book, the well-respected expert, Professor Lutz Tietze, summarizes the possibilities of this reaction type - an approach for an efficiant, economically benificial and ecological benign synthesis. A definite must for every organic chemist.