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Enantioselective Synthesis of Beta-Amino Acids
 
 
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Enantioselective Synthesis of Beta-Amino Acids [Hardcover]

Eusebio Juaristi (Editor), V. A. Soloshonok (Editor)

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Book Description

April 21, 2005
Covers all facets of the synthesis of ?-amino acids

As evidenced by an exponential increase in the literature published on the subject, interest in ?-amino acids has grown over the past several years. With major pharmaceutical applications, these amino acids are now studied across multiple lines of research, including combinatorial chemistry, medicinal chemistry, molecular design, proteomics, and others.

This Second Edition of Enantioselective Synthesis of ?-Amino Acids updates reviews included in the First Edition while also covering new developments since its publication. The book presents detailed discussions of the most important methods for the synthesis of ?-amino acids. In most cases, the lead chemist who originally developed a method provides an authoritative description of it.

In addition, Enantioselective Synthesis of ?-Amino Acids, Second Edition:
* Features introductory overviews on the structural types of relevant ?-amino acid targets and salient ?-amino acids present in natural products
* Dedicates several chapters to advances in the synthesis of oligomers from ?-amino acids
* Includes general and practical procedures for the preparation of ?-amino acids in each chapter
* Discusses the most important methods that have been recently developed for the asymmetric synthesis of cyclic and open-chain ?-amino acids
* Includes a report on the preparation of libraries of enantiopure ?-amino acids using combinatorial approaches

The only book of its kind available today, Enantioselective Synthesis of ?-Amino Acids, Second Edition offers upper-level students and professionals an essential resource for pharmaceutical development, medicinal chemistry, and biochemistry.

Editorial Reviews

Review

"…a 'must-have' handbook…it should be on the bookshelves of organic chemists in academia as well as in the pharmaceutical industry." (Journal of the American Chemical Society, October 26, 2005)

From the Back Cover

Covers all facets of the synthesis of β-amino acids

As evidenced by an exponential increase in the literature published on the subject, interest in β-amino acids has grown over the past several years. With major pharmaceutical applications, these amino acids are now studied across multiple lines of research, including combinatorial chemistry, medicinal chemistry, molecular design, proteomics, and others.

This Second Edition of Enantioselective Synthesis of β-Amino Acids updates reviews included in the First Edition while also covering new developments since its publication. The book presents detailed discussions of the most important methods for the synthesis of β-amino acids. In most cases, the lead chemist who originally developed a method provides an authoritative description of it.

In addition, Enantioselective Synthesis of β-Amino Acids, Second Edition:

  • Features introductory overviews on the structural types of relevant β-amino acid targets and salient β-amino acids present in natural products
  • Dedicates several chapters to advances in the synthesis of oligomers from β-amino acids
  • Includes general and practical procedures for the preparation of β-amino acids in each chapter
  • Discusses the most important methods that have been recently developed for the asymmetric synthesis of cyclic and open-chain β-amino acids
  • Includes a report on the preparation of libraries of enantiopure β-amino acids using combinatorial approaches

The only book of its kind available today, Enantioselective Synthesis of β-Amino Acids, Second Edition offers upper-level students and professionals an essential resource for pharmaceutical development, medicinal chemistry, and biochemistry.


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Inside This Book (learn more)
First Sentence:
The simplest -amino acid is -aminopropionic acid (-alanine, 1), which is not a proteinogenic amino acid, but it is an essential component of many relevant, biologically active compounds, such as vitamin B3 (pantothenic acid, 2). Read the first page
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
proteinogenic side chains, unmodified aldehydes, silicon enolates, nonenolizable aldehydes, diastereoselective conjugate addition, enantioselective conjugate addition, taxane anticancer agents, helical wheel diagrams, constrained residues, enantioselective synthesis, aminophosphonic acids, butyl butanoate, phosphonic acid derivatives, conjugate addition reactions, diastereoselective synthesis, protecting group manipulation, syn diastereomer, ammonia equivalent, chiral nonracemic, oxime ether, dialkyl phosphites, asymmetric synthesis, major diastereomer, silyl enolates, enzymatic resolution
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Tetrahedron Lett, New York, Perkin Trans, John Wiley, Second Edition Edited, Entry Substrate, Product Yield, Methods Based, American Chemical Society, Liebigs Ann, Boc Boc, Department of Chemistry, General Procedure, Symposium Series, L-proline-catalyzed Mannich-type, Liehigs Ann, Suresh Babu, Angew Chem, Cancer Inst, Stony Brook, University of Wisconsin-Madison, Boca Raton, Ochoa de Retana, Tetrahedron Asymmetry, Vander Velde
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