The carbonyl group is undoubtedly one of the most important functional groups in organic chemistry, both in its role as reactive center for synthesis or derivatisation and as crucial feature for special structural or physiological properties. Vast and profound progress has been made in all aspects modern carbonyl chemistry. These achievements are, however, rather dispersed in the literature and it is often not easy for the researcher obtain a comprehensive overview of a relevant topic. Modern Carbonyl Chemistry overcomes this inconvenience by collating the information for appropriate themes. In this work internationally renowned experts and leaders in the field have surveyed recent aspects and modern features in carbonyl chemistry, such as cascade-reactions, one-pot-syntheses, recognition, or site differentiation.
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Modern Carbobyl Chemistry Junzo Otera (Ed.) The carbonyl group is undoubtedly one of the most important functional groups in organic chemistry, both in its role as reactive center of synthesis or derivatisation and as crucial feature for special structural or physiological properties. Vast and profound progress has been made in all aspects of modern carbonyl chemistry. These achievements are, however, rather dispersed in the literature and it is often not easy for the researcher to obtain a comprehensive overview of a relevant topic. Modern Carbonyl Chemistry overcomes this inconvenience by collating the information for appropriate themes. In this work internationally renowned experts and leaders in the field have surveyed recent aspects and modern features in carbonyl chemistry, such as cascade-reactions, one-pot-synthesis, recognition, or site differentiation.
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Carbonyl is one of the commonest functional groups to be found in organic compounds and is often encountered in biomolecules such as peptides and lipids, playing a crucial role in organizing three-dimensional intermolecular associations [1]. Read the first page Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
crotylmetal reagents, indium reagents, synclinal transition state, allenylmetal reagents, crotylation reactions, relative stereoselection, syn aldol reaction, pinacol coupling reaction, chemoselective functionalization, sulfonyl oxime ethers, syn homoallylic alcohol, acyl radical cyclizations, allylborane reagents, pinacol cyclization, chiral allenylstannanes, chiral allylmetal, silicon electrofuge, syn transition structure, anti homoallylic alcohol, chiral activators, allylmetal reagents, antiperiplanar transition state, anti aldol reaction, acyclic transition structure, chiral diether Key Phrases - Capitalized Phrases (CAPs): (learn more)
Tetrahedron Lett, New York, Perkin Trans, Tetrahedron Asymm, Pergamon Press, Tetrahedron Len, Academic Press, Angew Chem, Pure Appl, Liebigs Ann, Study of Carbonyl-Lewis Acid Complexes, Entry Lewis, Methods of Organic Chemistry, Product Yield, Allylation of Carbonyls, Helu Chim, Hely Chim, Detailed Reaction Mechanisms, Osaka University, Recognition of Carbonyl Substrate, Ser Khim, Anti-Felkin Figure, Kluwer Academic Publishers, Nippon Kagaku Zassi, Pure Chem New!
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Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
Carbonyl is one of the commonest functional groups to be found in organic compounds and is often encountered in biomolecules such as peptides and lipids, playing a crucial role in organizing three-dimensional intermolecular associations [1]. Read the first page Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
crotylmetal reagents, indium reagents, synclinal transition state, allenylmetal reagents, crotylation reactions, relative stereoselection, syn aldol reaction, pinacol coupling reaction, chemoselective functionalization, sulfonyl oxime ethers, syn homoallylic alcohol, acyl radical cyclizations, allylborane reagents, pinacol cyclization, chiral allenylstannanes, chiral allylmetal, silicon electrofuge, syn transition structure, anti homoallylic alcohol, chiral activators, allylmetal reagents, antiperiplanar transition state, anti aldol reaction, acyclic transition structure, chiral diether Key Phrases - Capitalized Phrases (CAPs): (learn more)
Tetrahedron Lett, New York, Perkin Trans, Tetrahedron Asymm, Pergamon Press, Tetrahedron Len, Academic Press, Angew Chem, Pure Appl, Liebigs Ann, Study of Carbonyl-Lewis Acid Complexes, Entry Lewis, Methods of Organic Chemistry, Product Yield, Allylation of Carbonyls, Helu Chim, Hely Chim, Detailed Reaction Mechanisms, Osaka University, Recognition of Carbonyl Substrate, Ser Khim, Anti-Felkin Figure, Kluwer Academic Publishers, Nippon Kagaku Zassi, Pure Chem New!
Books on Related Topics | Concordance | Text Stats Browse Sample Pages:
Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
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This book cites 61
books:
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9
books
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- Organic Synthesis by B. Trost on 9 pages
- Asymmetric Catalysis In Organic Synthesis (Baker Lecture Series) by Ryoji Noyori on 4 pages
- Catalytic Asymmetric Synthesis, Second Edition by Iwao Ojima on page 220, page 247, and page 395
- Advances in Detailed Reaction Mechanisms: v. 4 by J.M. Coxon on page 183, page 184, and page 395
- Organic Synthesis by Michael B Smith on page 89, and page 562
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- Modern Aldol Reactions (2 Volume Set) by Rainer Mahrwald on page 319, and page 323
- Boronic Acids: Preparation and Applications in Organic Synthesis and Medicine by Dennis G. Hall on page 96, and page 254
- Fundamentals of Molecular Catalysis, Volume 3 (Current Methods in Inorganic Chemistry) by Hideo Kurosawa on page 472
- Advanced Organic Chemistry: Reaction Mechanisms (Advanced Organic Chemistry Series) by Reinhard Bruckner on page 346
- Advances in Heterocyclic Chemistry, Volume 92 by Alan R. Katritzky on page 214
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