Incorporation of heterocycles into combinatorial chemistry /

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Bibliographic Details
Author / Creator:Babaev, Eugene V., author.
Imprint:[Cham, Switzerland] : Springer, 2017.
©2017
Description:1 online resource (123 pages) : illustrations, tables
Language:English
Series:SpringerBriefs in molecular science
SpringerBriefs in molecular science.
Subject:
Format: E-Resource Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/11270374
Hidden Bibliographic Details
ISBN:9783319500157
3319500155
9783319500133
3319500139
Digital file characteristics:text file PDF
Notes:Includes bibliographical references.
Summary:The author has summarized a decade of teaching combinatorial chemistry into this timely brief. The solid phase synthesis of unnatural heterocyclic alpha-amino acids is illustrated by practical examples starting from the ABCs of peptide synthesis explored in chapter one. Chapter two is concerned with the solid phase synthesis which is shown on various techniques - BillBoard, tea-bag, and Lantern devices, and demonstrated on heterocyclic examples and protocols. In the third chapter the tools for accelerating chemical synthesis - solid phase and liquid phase - are reviewed. Here the techniques of parallel refluxing (including microwave and flow technique) and parallel separation (filtration, centrifugation, evaporation, and chromatography) are described. In the chapters 4 and 5 the author goes on to describe how the liquid phase synthesis of heterocycles (reductive amination and Ugi reaction of heterocycles) is illustrated with the use of semi-automated protocols. Finally, the design of combinatorial libraries of heterocycles is reviewed including the original author's findings.
Other form:Print version: Babaev, Eugene V. Incorporation of heterocycles into combinatorial chemistry. [Cham, Switzerland] : Springer, 2017 3319500139 9783319500133
Standard no.:10.1007/978-3-319-50015-7

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505 0 |a Introduction -- Peptide Synthesis of Libraries of Non-Natural Amino Acids -- The choice of tools for implementing multi-stage transformations. SPOS for Beginners -- Secrets of Parallel Liquid-Phase Synthesis -- Most Combinatorial LPOS Reactions: Reductive Amination with a Scavenger -- A Parallel Ugi Reaction -- Combinatorial Heterocyclic Chemistry in Higher School. 
520 |a The author has summarized a decade of teaching combinatorial chemistry into this timely brief. The solid phase synthesis of unnatural heterocyclic alpha-amino acids is illustrated by practical examples starting from the ABCs of peptide synthesis explored in chapter one. Chapter two is concerned with the solid phase synthesis which is shown on various techniques - BillBoard, tea-bag, and Lantern devices, and demonstrated on heterocyclic examples and protocols. In the third chapter the tools for accelerating chemical synthesis - solid phase and liquid phase - are reviewed. Here the techniques of parallel refluxing (including microwave and flow technique) and parallel separation (filtration, centrifugation, evaporation, and chromatography) are described. In the chapters 4 and 5 the author goes on to describe how the liquid phase synthesis of heterocycles (reductive amination and Ugi reaction of heterocycles) is illustrated with the use of semi-automated protocols. Finally, the design of combinatorial libraries of heterocycles is reviewed including the original author's findings. 
504 |a Includes bibliographical references. 
650 0 |a Heterocyclic chemistry.  |0 http://id.loc.gov/authorities/subjects/sh86007058 
650 0 |a Combinatorial chemistry.  |0 http://id.loc.gov/authorities/subjects/sh96005121 
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650 7 |a Organic chemistry.  |2 bicssc 
650 7 |a Combinatorial chemistry.  |2 fast  |0 (OCoLC)fst00868966 
650 7 |a Heterocyclic chemistry.  |2 fast  |0 (OCoLC)fst00955735 
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