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The Organic Chemistry of Sugars
 
 
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The Organic Chemistry of Sugars [Hardcover]

Daniel E. Levy (Editor), Péter Fügedi (Editor)
4.0 out of 5 stars  See all reviews (1 customer review)

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Book Description

September 21, 2005 0824753550 978-0824753559 1
Intrigued as much by its complex nature as by its outsider status in traditional organic chemistry, the editors of The Organic Chemistry of Sugars compile a groundbreaking resource in carbohydrate chemistry that illustrates the ease at which sugars can be manipulated in a variety of organic reactions.

Each chapter contains numerous examples demonstrating the methods and strategies that apply mainstream organic chemistry to the chemical modification of sugars. The book first describes the discovery, development, and impact of carbohydrates, followed by a discussion of protecting group strategies, glycosylation techniques, and oligosaccharide syntheses. Several chapters focus on reactions that convert sugars and carbohydrates to non-carbohydrate molecules including the substitution of sugar hydroxyl groups to new groups of synthetic or biological interest, cyclitols and carbasugars, as well as endocyclic heteroatom substitutions. Subsequent chapters demonstrate the use of sugars in chiral catalysis, their roles as convenient starting materials for complex syntheses involving multiple stereogenic centers, and syntheses for monosaccharides. The final chapters focus on new and emerging technologies, including approaches to combinatorial carbohydrate chemistry, the biological importance and chemical synthesis of glycopeptides, and the medicinally significant concept of glycomimetics.

Presenting the organic chemistry of sugars as a solution to many complex synthetic challenges, The Organic Chemistry of Sugars provides a comprehensive treatment of the manipulation of sugars and their importance in mainstream organic chemistry.

Daniel E. Levy, editor of the Drug Discovery Series, is the founder of DEL BioPharma, a consulting service for drug discovery programs. He also maintains a blog that explores organic chemistry.


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Product Details

  • Hardcover: 904 pages
  • Publisher: CRC Press; 1 edition (September 21, 2005)
  • Language: English
  • ISBN-10: 0824753550
  • ISBN-13: 978-0824753559
  • Product Dimensions: 10 x 7.1 x 2.1 inches
  • Shipping Weight: 3.8 pounds (View shipping rates and policies)
  • Average Customer Review: 4.0 out of 5 stars  See all reviews (1 customer review)
  • Amazon Best Sellers Rank: #2,189,334 in Books (See Top 100 in Books)

More About the Author

DANIEL E. LEVY, PhD was born in 1965 in San Francisco, CA. From an early age, he demonstrated a strong interest in chemistry and a desire to improve the quality of patients' lives by contributing to the discovery of new therapeutic agents.

While pursuing his undergraduate degree at the University of California - Berkeley, Dr. Levy explored all opportunities to participate in organic chemistry research and to develop his laboratory skills. Under the supervision of Professor Henry Rapoport, he contributed to projects including the synthesis of novel analogs of pilocarpine and the synthesis of 4-amino-4-deoxy sugars from amino acids.

Following the completion of his bachelor's of science in 1987, Dr. Levy pursued his Ph.D. at the Massachusetts Institute of Technology. Under the direction of Professor Satoru Masamune, Dr. Levy completed a thesis entitled "Towards the Synthesis of Calyculin A."

After receiving his Ph.D. in 1992, Dr. Levy contributed to biotechnology companies pursuing novel therapeutics for the treatment of inflammation, cancer and cardiovascular diseases. He held positions at companies including Glycomed, COR Therapeutics and Scios. Dr. Levy is currently the director of synthetic chemistry at Intradigm corporation where he is pursuing novel delivery vehicles for siRNA therapeutics. He is also the founder of DEL Biopharma providing consulting services to the biopharmaceutical industry.

In 1995, Dr. Levy coauthored with Dr. Cho Tang a book entitled "The Chemistry of C-Glycosides" and later collaborated with Dr. Peter Fugedi in the development and presentation of short courses entitled "Modern Synthetic Carbohydrate Chemistry" and "The Organic Chemistry of Sugars" offered by the American Chemical Society Continuing Education Department. In 2005, Dr. Levy coedited with Dr. Fugedi the book "The Organic Chemistry of Sugars" based on the short course of the same name.

Through his studies, Dr. Levy noticed that many organic chemistry students rely on memorization of the vast number of reactions taught in introductory courses. It was this observation that motivated him to write "Arrow Pushing in Organic Chemisty: An Easy Approach to Understanding Reaction Mechanisms." This book, published in 2008, began as an outline of his approach to study and tutor organic chemistry. It is designed to teach strategies that minimize memorization and increase understanding. The goal of this supplementary text is to retain and motivate more students in the pursuit of organic chemistry and related disciplines. "Arrow Pushing in Organic Chemistry" is dedicated to the memory of Professor Henry Rapoport.

 

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4.0 out of 5 stars Organic Chemistry of Sugars, July 21, 2011
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This review is from: The Organic Chemistry of Sugars (Hardcover)
Excellent book for organic chemists who want to learn synthesis of sugars and polysaccharides. It provides great detail about protecting group strategies, and has numerous examples of carbohydrates in drug discovery.
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Inside This Book (learn more)
First Sentence:
Figure 1.1 shows this writer's perspective of the developmental phases of the subject of this book. Read the first page
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
carbohydrate auxiliaries, artificial glycopeptide libraries, aglycon derivative, artificial glycopeptides, antigen building blocks, adjacent coplanar atoms, glycosyl trifluoroacetimidates, bidesmosidic triterpene saponin, carbohydrate auxiliary, destomic acid, anomeric activating groups, chlorosulfate esters, anomeric carbenes, naked sugars, aglycone delivery, griseolic acid, trisaccharide block, anomeric anions, dehydrative glycosylation, threonine building blocks, glycosyl sulfonates, intramolecular glycosidation, orthogonal glycosylation strategy, sugar auxiliary, glycopeptide synthesis
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Tetrahedron Lett, New York, Liebigs Ann, Perkin Trans, Emil Fischer, Pure Appl, Liehigs Ann, Marcel Dekker, Acta Chem, Tetrahedron Asymmetry, Methods Carbohydr, Promoter Ref, Academic Press, Creation of C-Glycosidic Bonds, Pergamon Press, Rama Rao, Burckhardt Helferich, Hermann Fischer, Oxford University Press, Agents Chemother, American Chemical Society, Intramolecular O-glycoside, Nobel Prize, Diabetes Care, Diabetes Metab
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